Variant #0000719213 (NC_000003.11:g.136060343T>C, NM_000532.4:c.*11475T>C (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.136060343T>C
DNA change (hg38) -
Published as STAG1(NM_005862.3):c.3497A>G (p.N1166S)
ISCN -
DB-ID STAG1_000019
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.*11475T>C r.(=) p.(=)
STAG1 NM_005862.2 ?/. - c.3497A>G r.(?) p.(Asn1166Ser)


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