Variant #0000924487 (NC_000006.11:g.32814929C>T, NM_000593.5:c.2136G>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.32814929C>T
DNA change (hg38) -
Published as TAP1(NM_000593.5):c.2136G>A (p.A712=)
ISCN -
DB-ID PSMB8_000052
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) 8.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP1 NM_000593.5 -?/. - c.2136G>A r.(?) p.(Ala712=)
PSMB8 NM_148919.3 -?/. - c.-3156G>A r.(?) p.(=)


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