Variant #0001014395 (NC_000007.13:g.99796885C>T, NM_012447.2:c.1468C>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.99796885C>T
DNA change (hg38) -
Published as STAG3(NM_012447.4):c.1468C>T (p.L490F)
ISCN -
DB-ID PVRIG_000015
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) 0.00021 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +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     
STAG3 NM_012447.2 ?/. - c.1468C>T r.(?) p.(Leu490Phe)
PVRIG NM_024070.3 ?/. - c.-20337C>T r.(?) p.(=)
GATS NM_178831.6 ?/. - c.*3390G>A r.(=) p.(=)


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