Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

12 entries on 1 page. Showing entries 1 - 12.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
-/. - c.4805G>A r.(?) p.(Arg1602Gln) - Unknown - benign g.76910816G>A g.77199771G>A MYO7A(NM_000260.3):c.4805G>A (p.(Arg1602Gln)) - MYO7A_000149 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Pennings 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2006 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Pennings 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2006 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Liu 1998; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - ? ? PubMed: Liu 1998 Proband F - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Parent #1 ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Heterozygous PubMed: Liu 1998; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs139889944 Germline - - - - - DNA SEQ - - ? ? PubMed: Liu 1998 Relative M - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
-/? 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Paternal (inferred) ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Homozygous Weston 1998, Assoc Res Otolaryngol Abs, p. 46, 1998 - rs139889944 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? Weston 1998, Assoc Res Otolaryngol Abs, p. 46, 1998 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 35 c.4805G>A r.(?) p.(Arg1602Gln) FERM 1 (1258-1602) Maternal (inferred) ACMG likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 Homozygous Weston 1998, Assoc Res Otolaryngol Abs, p. 46, 1998 - rs139889944 Germline - 0/192 controls - - - DNA SEQ - - USH1B ? Weston 1998, Assoc Res Otolaryngol Abs, p. 46, 1998 Proband - - United States - - - - - 1 William J. Kimberling
-?/. - c.4805G>A r.(?) p.(Arg1602Gln) - Unknown - likely benign g.76910816G>A g.77199771G>A MYO7A(NM_000260.3):c.4805G>A (p.(Arg1602Gln)) - MYO7A_000149 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.4805G>A r.(?) p.(Arg1602Gln) - Parent #1 - likely benign g.76910816G>A g.77199771G>A - - MYO7A_000149 7 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs139889944 Germline - 7/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 7 Mohammed Faruq
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