Variant #0000621699 (NC_000006.11:g.32823983G>A, NM_000593.5:c.-2390C>T (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.32823983G>A
DNA change (hg38) g.32856206G>A
Published as PSMB9(NM_002800.5):c.128+1G>A
ISCN -
DB-ID PSMB9_000012
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP1 NM_000593.5 ?/. - c.-2390C>T r.(?) p.(=)
PSMB9 NM_002800.4 ?/. - c.128+1G>A r.spl? p.?


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