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.

3 entries on 1 page. Showing entries 1 - 3.
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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.1764G>A r.(spl?) p.(Trp588*) - Unknown - pathogenic g.75435758G>A g.72820842G>A - - TMC1_000042 - PubMed: Sommen 2016, Journal: Sommen 2016 - rs18259073 Germline - - - - - DNA SEQ, SEQ-NG-I - - DFNB;ARNSHL - PubMed: Sommen 2016, Journal: Sommen 2016 - - - - - - - - - 1 Manou Sommen
+/+ 20 c.1764G>A r.(?) p.(Trp588*) - Paternal (inferred) ACMG VUS g.75435758G>A g.72820842G>A - - TMC1_000042 homozygous; Pathogenic PubMed: Tlili 2008 - - Germline - 0/200 controls +XbaI;+Hpy188III;-BtsCI;-BccI;-FokI - - DNA SEQ - - DFNB - PubMed: Tlili 2008 Proband F - Tunisia - - - - - 1 Anne-Françoise Roux
+/+ 20 c.1764G>A r.(?) p.(Trp588*) - Maternal (inferred) ACMG VUS g.75435758G>A g.72820842G>A - - TMC1_000042 homozygous; Pathogenic PubMed: Tlili 2008 - - Germline - 0/200 controls +XbaI;+Hpy188III;-BtsCI;-BccI;-FokI - - DNA SEQ - - DFNB - PubMed: Tlili 2008 Proband F - Tunisia - - - - - 1 Anne-Françoise Roux
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