Variant #0000930894 (NC_000017.10:g.76117783C>G, NM_007267.6:c.1237G>C (TMC6))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76117783C>G
DNA change (hg38) -
Published as TMC6(NM_007267.6):c.1237G>C (p.A413P), TMC6(NM_007267.7):c.1237G>C (p.A413P)
ISCN -
DB-ID TMC8_000059 See all 2 reported entries
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) 0.00071 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 2023-07-07 10:10:56 +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.1237G>C r.(?) p.(Ala413Pro)
TMC8 NM_152468.4 -?/. - c.-9458C>G r.(?) p.(=)


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