Full data view for gene CLRN1


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the transcript reference sequence.

87 entries on 1 page. Showing entries 1 - 87.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

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+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Parent #1 - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Adato 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 1/220 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Adato 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband M - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Parent #1 - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband M - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Fields 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/200 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Fields 2002 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ness 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 3/838 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ness 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - RPar - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Parent #1 - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Unknown - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Unknown - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - RPar - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Herrera 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Herrera 2008 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Isosomppi 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Isosomppi 2009 Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Isosomppi 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Isosomppi 2009 Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Parent #1 - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Isosomppi 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Isosomppi 2009 Proband - - Finland - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous; Pathogenic PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/878 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous; Pathogenic PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - 0/878 controls +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Parent #1 - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous PubMed: Ratnam 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ratnam 2012 Proband M - Finland - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ratnam 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ratnam 2012 Proband F - Finland - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Paternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ratnam 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ratnam 2012 Proband F - Finland - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ratnam 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ratnam 2012 Proband F - Finland - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Maternal (inferred) - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 homozygous PubMed: Ratnam 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - +PhoI;+StuI;+HaeIII;+CviKI_1; - - DNA SEQ - - USH3 - PubMed: Ratnam 2012 Proband F - Finland - - - - - 1 Anne-Françoise Roux
+/+ 1 c.144T>G r.(?) p.(Asn48Lys) - Parent #2 - pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033258 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.144T>G r.(?) p.(Asn48Lys) - Unknown - pathogenic (recessive) g.150690352A>C - 3:150690352A>C ENST00000328863.4:c.144T>G (Asn48Lys) - CLRN1_000007 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240033 PubMed: Carss 2017 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.144T>G r.(?) p.(Asn48Lys) - Both (homozygous) - likely pathogenic g.150690352A>C g.150972565A>C CLRN1(USH3A);NM_001195794.1;c.[144T>G];[144T>G]p.[(Asn48Lys)];[(Asn48Lys)] - CLRN1_000007 homozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 105 genes panel retinal disease 17 PubMed: Jiman 2020 - F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.144T>G r.(?) p.(Asn48Lys) - Both (homozygous) - likely pathogenic g.150690352A>C g.150972565A>C CLRN1 c.144T>G, p.N48K - CLRN1_000007 homozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 155 PubMed: Jauregui 2020 - F - (United States) white - - - - 1 LOVD
+?/. - c.144T>G r.(?) p.(Asn48Lys) - Both (homozygous) - likely pathogenic g.150690352A>C g.150972565A>C CLRN1 c.144T>G, p.N48K - CLRN1_000007 homozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 156 PubMed: Jauregui 2020 - M - (United States) white - - - - 1 LOVD
+?/+? 01 c.144T>G r.(?) p.(Asn48Lys) - Unknown ACMG likely pathogenic g.150690352A>C g.150972565A>C - - CLRN1_000007 PS3_M, PM3_VS - - rs111033258 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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