Variant #0000314534 (NC_000017.10:g.76130987G>T, NM_007267.6:c.-2640C>A (TMC6))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76130987G>T
DNA change (hg38) g.78134906G>T
Published as TMC8(NM_152468.4):c.1024G>T (p.G342W)
ISCN -
DB-ID TMC8_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02458 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMC6 NM_007267.6 -/. - c.-2640C>A r.(?) p.(=)
TMC8 NM_152468.4 -/. - c.1024G>T r.(?) p.(Gly342Trp)


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