Variant #0000894312 (NC_000017.10:g.76109657C>T, NM_007267.6:c.2326G>A (TMC6))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76109657C>T
DNA change (hg38) -
Published as TMC6(NM_007267.7):c.2326G>A (p.E776K)
ISCN -
DB-ID TMC8_000073
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.2326G>A r.(?) p.(Glu776Lys)
TNRC6C NM_018996.3 ?/. - c.*8731C>T r.(=) p.(=)
TMC8 NM_152468.4 ?/. - c.-17584C>T r.(?) p.(=)


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