Variant #0000858813 (NC_000003.11:g.135978028G>T, NC_000003.11(NM_000532.4):c.373-1293G>T (PCCB))

Chromosome 3
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.135978028G>T
DNA change (hg38) -
Published as PCCB(NM_001178014.1):c.383G>T (p.G128V)
ISCN -
DB-ID STAG1_000046
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCCB NM_000532.4 ?/. - c.373-1293G>T r.(=) p.(=)
STAG1 NM_005862.2 ?/. - c.*79068C>A r.(=) p.(=)


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