Variant #0000528594 (NC_000006.11:g.32818212C>T, NM_000593.5:c.1313G>A (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.32818212C>T
DNA change (hg38) g.32850435C>T
Published as TAP1(NM_000593.5):c.1313G>A (p.R438Q), TAP1(NM_000593.6):c.1133G>A (p.R378Q)
ISCN -
DB-ID PSMB9_000001 See all 2 reported entries
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) 6.0E-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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP1 NM_000593.5 ?/. - c.1313G>A r.(?) p.(Arg438Gln)
PSMB9 NM_002800.4 ?/. - c.-3795C>T r.(?) p.(=)


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