Variant #0000654812 (NC_000003.11:g.136047711_136047712del, NC_000003.11(NM_000532.4):c.1498+12_1498+13del (PCCB))

Chromosome 3
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.136047711_136047712del
DNA change (hg38) g.136328869_136328870del
Published as PCCB(NM_001178014.1):c.1558+12_1558+13delTG
ISCN -
DB-ID STAG1_000028
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 2020-03-23 16:13:27 +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     
PCCB NM_000532.4 -?/. - c.1498+12_1498+13del r.(=) p.(=)
STAG1 NM_005862.2 -?/. - c.*9386_*9387del r.(=) p.(=)


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