Variant #0000689711 (NC_000006.11:g.32810752C>G, NM_000593.5:c.*2604G>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.32810752C>G
DNA change (hg38) -
Published as PSMB8(NM_004159.5):c.250G>C (p.V84L)
ISCN -
DB-ID PSMB8_000035
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) 0 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP2 NM_000544.3 ?/. - c.-4327G>C r.(?) p.(=)
TAP1 NM_000593.5 ?/. - c.*2604G>C r.(=) p.(=)
PSMB8 NM_148919.3 ?/. - c.262G>C r.(?) p.(Val88Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.