Variant #0000518046 (NC_000003.11:g.135978029C>T, NC_000003.11(NM_000532.4):c.373-1292C>T (PCCB))

Chromosome 3
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.135978029C>T
DNA change (hg38) g.136259187C>T
Published as PCCB(NM_001178014.2):c.384C>T (p.G128=)
ISCN -
DB-ID STAG1_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) 0.00255 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
PCCB NM_000532.4 -/. - c.373-1292C>T r.(=) p.(=)
STAG1 NM_005862.2 -/. - c.*79067G>A r.(=) p.(=)


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