Variant #0000803330 (NC_000007.13:g.99801713T>C, NM_012447.2:c.2770T>C (STAG3))

Chromosome 7
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.99801713T>C
DNA change (hg38) -
Published as STAG3(NM_001282717.1):c.2770T>C (p.C924R)
ISCN -
DB-ID PVRIG_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) 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAG3 NM_012447.2 ?/. - c.2770T>C r.(?) p.(Cys924Arg)
PVRIG NM_024070.3 ?/. - c.-15509T>C r.(?) p.(=)
GATS NM_178831.6 ?/. - c.*49-1487A>G r.(=) p.(=)


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