Variant #0000860308 (NC_000006.11:g.32819922G>A, NM_000593.5:c.988C>T (TAP1))

Chromosome 6
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.32819922G>A
DNA change (hg38) -
Published as TAP1(NM_000593.5):c.988C>T (p.R330C)
ISCN -
DB-ID PSMB9_000020
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP1 NM_000593.5 ?/. - c.988C>T r.(?) p.(Arg330Cys)
PSMB9 NM_002800.4 ?/. - c.-2085G>A r.(?) p.(=)


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