Variant #0000912481 (NC_000006.11:g.32810001C>T, NM_000593.5:c.*3355G>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.32810001C>T
DNA change (hg38) -
Published as PSMB8(NM_148919.4):c.447G>A (p.S149=)
ISCN -
DB-ID PSMB8_000050
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) 5.0E-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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP2 NM_000544.3 -?/. - c.-3576G>A r.(?) p.(=)
TAP1 NM_000593.5 -?/. - c.*3355G>A r.(=) p.(=)
PSMB8 NM_148919.3 -?/. - c.447G>A r.(?) p.(Ser149=)


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