Variant #0000306560 (NC_000006.11:g.32809425C>T, NM_000593.5:c.*3931G>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.32809425C>T
DNA change (hg38) g.32841648C>T
Published as PSMB8(NM_004159.5):c.613G>A (p.G205R), PSMB8(NM_148919.3):c.625G>A (p.(Gly209Arg))
ISCN -
DB-ID PSMB8_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP2 NM_000544.3 ?/. - c.-3000G>A r.(?) p.(=)
TAP1 NM_000593.5 ?/. - c.*3931G>A r.(=) p.(=)
PSMB8 NM_148919.3 ?/. - c.625G>A r.(?) p.(Gly209Arg)


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