Variant #0000982825 (NC_000017.10:g.76117158G>A, NM_007267.6:c.1471C>T (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.76117158G>A
DNA change (hg38) -
Published as TMC6(NM_007267.6):c.1471C>T (p.R491C)
ISCN -
DB-ID TMC8_000087
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) 0.00116 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMC6 NM_007267.6 -/. - c.1471C>T r.(?) p.(Arg491Cys)
TMC8 NM_152468.4 -/. - c.-10083G>A r.(?) p.(=)


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