Variant #0000315766 (NC_000007.13:g.99778263T>C, NM_012447.2:c.84T>C (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.99778263T>C
DNA change (hg38) g.100180640T>C
Published as STAG3(NM_001282717.1):c.84T>C (p.F28=)
ISCN -
DB-ID STAG3_000006
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-23 10:58:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAG3 NM_012447.2 -?/. - c.84T>C r.(?) p.(Phe28=)
GPC2 NM_152742.1 -?/. - c.-3441A>G r.(?) p.(=)
GATS NM_178831.6 -?/. - c.*22012A>G r.(=) p.(=)


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