Variant #0000533189 (NC_000007.13:g.99808701C>G, NM_012447.2:c.3306C>G (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.99808701C>G
DNA change (hg38) g.100211078C>G
Published as STAG3(NM_001282717.1):c.3306C>G (p.I1102M), STAG3(NM_012447.2):c.3306C>G (p.(Ile1102Met))
ISCN -
DB-ID PVRIG_000002 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAG3 NM_012447.2 -?/. - c.3306C>G r.(?) p.(Ile1102Met)
PVRIG NM_024070.3 -?/. - c.-8521C>G r.(?) p.(=)
GATS NM_178831.6 -?/. - c.*49-8475G>C r.(=) p.(=)


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