Variant #0001036639 (NC_000007.13:g.99808689G>T, NM_012447.2:c.3294G>T (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.99808689G>T
DNA change (hg38) -
Published as STAG3(NM_001282717.2):c.3294G>T (p.(Gln1098His))
ISCN -
DB-ID PVRIG_000016
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) 0.00034 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAG3 NM_012447.2 ?/. - c.3294G>T r.(?) p.(Gln1098His)
PVRIG NM_024070.3 ?/. - c.-8533G>T r.(?) p.(=)
GATS NM_178831.6 ?/. - c.*49-8463C>A r.(=) p.(=)


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