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.

11 entries on 1 page. Showing entries 1 - 11.
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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     
?/? 3 c.-258A>C r.(?) p.(?) - Paternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Proband M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Paternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Paternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Paternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Paternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Maternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Proband M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Maternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) - Maternal (inferred) - VUS g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) Cytoplasmic 1 (1-199);Highly Charged (4-178) Maternal (inferred) - pathogenic g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative M - Iran - - - - - 1 Anne-Françoise Roux
?/? 3 c.-258A>C r.(?) p.(?) Cytoplasmic 1 (1-199);Highly Charged (4-178) Maternal (inferred) - pathogenic g.75231331A>C g.72616415A>C g.94615A>C - TMC1_000003 homozygous; pathogenicity unclear, segregates with the disease PubMed: Hilgert 2008 - - Germline - 0/400 controls +DpnI;+Sau3AI;+MboI;+BfuCI;+DpnII;+TaqI - - DNA SEQ - - DFNB - PubMed: Hilgert 2008 Relative F - Iran - - - - - 1 Anne-Françoise Roux
-/- 1 c.-258A>C r.(=) p.(=) - Both (homozygous) ACMG benign g.75231331A>C g.72616415A>C - - TMC1_000003 Marker associated to the c.627C>T splicing alteration Vaché et al., submitted - rs937270834 Germline - - - - - DNA SEQ, SEQ-NG-I blood - DFNB7 FR01199350441 Vaché et al., submitted - M yes - - - - - - 1 David Baux
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