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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.1705A>G r.(?) p.(Thr569Ala) - Unknown - likely benign g.75431068A>G - TMC1(NM_138691.2):c.1705A>G (p.T569A), TMC1(NM_138691.3):c.1705A>G (p.(Thr569Ala)) - TMC1_000133 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1705A>G r.(?) p.(Thr569Ala) - Parent #1 - likely benign g.75431068A>G g.72816152A>G - - TMC1_000133 variant found in in normal hearing individuals PubMed: Ozieblo 2019 - - Germline no - - - - DNA SEQ, SEQ-NG - - DFNA family PubMed: Ozieblo 2019 5-generation family, 13 affected (5F, 8M) F;M - Poland - - - - - 13 Johan den Dunnen
?/. - c.1705A>G r.(?) p.(Thr569Ala) - Unknown - VUS g.75431068A>G - TMC1(NM_138691.2):c.1705A>G (p.T569A), TMC1(NM_138691.3):c.1705A>G (p.(Thr569Ala)) - TMC1_000133 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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