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.

2 entries on 1 page. Showing entries 1 - 2.
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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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

Template     

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Tissue     

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Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Owner     
+/. 15 c.1210T>C r.(?) p.(Trp404Arg) - Paternal (confirmed) - pathogenic g.75404219T>C g.72789303T>C - - TMC1_000040 - PubMed: Brownstein 2011, Journal: Brownstein 2011 - - Germline yes 2/168 cases (het) - - - DNA SEQ-NG-I blood - DFNB7 - PubMed: Brownstein 2011, Journal: Brownstein 2011 2-generation family, 3 affected sibs (2F, M), unaffected heterozygous carrier parents/sibs F;M no Israel Morocco;Jewish - - - - 3 Zippi Brownstein
?/? 15 c.1210T>C r.(?) p.(Trp404Arg) Cytoplasmic 1 (1-199) Paternal (confirmed) - pathogenic g.75404219T>C g.72789303T>C - - TMC1_000040 heterozygous; Possibly pathogenic PubMed: Brownstein 2011; USMA-missense variant in MSV3d - - Germline - 0/164 controls +FauI;+AciI - - DNA SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Proband F - Morocco - - - - - 1 Anne-Françoise Roux
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