Variant #0000563263 (NC_000017.10:g.76117727C>A, NM_007267.6:c.1293G>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.76117727C>A
DNA change (hg38) g.78121646C>A
Published as TMC6(NM_001127198.2):c.1293G>T (p.A431=)
ISCN -
DB-ID TMC6_000031
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 13:19:43 +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.1293G>T r.(?) p.(Ala431=)
TMC8 NM_152468.4 -?/. - c.-9514C>A r.(?) p.(=)


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