Variant #0000611139 (NC_000007.13:g.56126175_56126176del, NM_001762.3:c.846_847del (CCT6A))

Chromosome 7
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.56126175_56126176del
DNA change (hg38) g.56058482_56058483del
Published as CCT6A(NM_001762.4):c.846_847delTG (p.C282Wfs*5)
ISCN -
DB-ID CCT6A_000005
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-22 17:29:16 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCT6A NM_001762.3 ?/. - c.846_847del r.(?) p.(Cys282TrpfsTer5)


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