Full data view for gene TMC1


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_138691.2 transcript reference sequence.

14 entries on 1 page. Showing entries 1 - 14.
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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     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 20 c.1810C>T r.(?) p.(Arg604*) - Paternal (confirmed) - pathogenic g.75435804C>T g.72820888C>T - - TMC1_000001 0/128 controls - - - Germline yes 8/158 patients het - - - DNA SEQ-NG-I blood - DFNB7 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Ashkenazi;Algeria - - - - 2 Zippi Brownstein
+/. 20 c.1810C>T r.(?) p.(Arg604*) - Paternal (confirmed) - pathogenic g.75435804C>T g.72820888C>T - - TMC1_000001 not in 128 controls PubMed: Brownstein 2011, Journal: Brownstein 2011 - - Germline yes 8/168 cases (het) - - - DNA SEQ-NG-I blood - DFNB7 - PubMed: Brownstein 2011, Journal: Brownstein 2011 3-generation family, 4 affected3 (F, 3M), unaffected heterozygous carrier parents/sibs F;M no Israel Morocco;Jewish - - - - 4 Zippi Brownstein
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Paternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Proband M - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Paternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Paternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Paternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Paternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Maternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Proband M - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Maternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Maternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) Cytoplasmic 3 (462-634) Maternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) - Maternal (inferred) - pathogenic g.75435804C>T g.72820888C>T 2350C>T p.R604X - TMC1_000001 homozygous; Pathogenic PubMed: Hilgert 2008 - - Germline - - -HpyAV;-TaqI; - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Greece - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1810C>T r.(?) p.(Arg604*) - Paternal (confirmed) - pathogenic g.75435804C>T g.72820888C>T - - TMC1_000001 heterozygous; Pathogenic PubMed: Brownstein 2011 - - Germline - 0/256 controls -HpyAV;-TaqI; - - DNA SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
+/. - c.1810C>T r.(?) p.(Arg604Ter) - Paternal (confirmed) - pathogenic (recessive) g.75435804C>T g.72820888C>T - - TMC1_000001 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL PKDF/PKSR13b PubMed: Richard 2019 2-generation family, 6 affected sibs (3F, 3M) - yes Pakistan - - - - - 6 Johan den Dunnen
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