Variant #0000690119 (NC_000007.13:g.99802331C>T, NM_012447.2:c.2884C>T (STAG3))

Chromosome 7
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.99802331C>T
DNA change (hg38) -
Published as STAG3(NM_012447.2):c.2884C>T (p.(Arg962Trp))
ISCN -
DB-ID PVRIG_000009
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) 0.00062 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +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.2884C>T r.(?) p.(Arg962Trp)
PVRIG NM_024070.3 -?/. - c.-14891C>T r.(?) p.(=)
GATS NM_178831.6 -?/. - c.*49-2105G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.