Variant #0000311703 (NC_000006.11:g.32818774T>C, NM_000593.5:c.1177A>G (TAP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32818774T>C
DNA change (hg38) g.32850997T>C
Published as TAP1(NM_000593.6):c.997A>G (p.I333V)
ISCN -
DB-ID TAP1_000008
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) 0.20016 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP1 NM_000593.5 -/. - c.1177A>G r.(?) p.(Ile393Val)
PSMB9 NM_002800.4 -/. - c.-3233T>C r.(?) p.(=)


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