Variant #0000851192 (NC_000006.11:g.32810027G>T, NM_000593.5:c.*3329C>A (TAP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32810027G>T
DNA change (hg38) -
Published as PSMB8(NM_004159.5):c.409C>A (p.R137=)
ISCN -
DB-ID PSMB8_000044
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) 1.0E-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 2022-05-09 15:40:45 +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.-3602C>A r.(?) p.(=)
TAP1 NM_000593.5 -?/. - c.*3329C>A r.(=) p.(=)
PSMB8 NM_148919.3 -?/. - c.421C>A r.(?) p.(Arg141=)


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