Variant #0000316664 (NC_000017.10:g.76136926G>A, NM_007267.6:c.-8579C>T (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.76136926G>A
DNA change (hg38) g.78140845G>A
Published as TMC8(NM_152468.4):c.1914G>A (p.E638=)
ISCN -
DB-ID TMC8_000015
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 13:28:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMC6 NM_007267.6 -?/. - c.-8579C>T r.(?) p.(=)
TMC8 NM_152468.4 -?/. - c.1914G>A r.(?) p.(Glu638=)


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