Variant #0000887203 (NC_000006.11:g.32821499C>G, NM_000593.5:c.95G>C (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.32821499C>G
DNA change (hg38) -
Published as TAP1(NM_000593.5):c.95G>C (p.G32A)
ISCN -
DB-ID PSMB9_000023
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.95G>C r.(?) p.(Gly32Ala)
PSMB9 NM_002800.4 ?/. - c.-508C>G r.(?) p.(=)


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