RGD:41407323 Rat Genome Database

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Variant: RGD:41407323 -  Homo sapiens

RGD ID: 41407323
RS ID: rs200932463
ClinVar ID: CV981570
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIK3CG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 106,523,628
GRCh38 7 106,883,183
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282426.2:c.2760+20C>T
NM_001282427.2:c.2760+20C>T
NM_002649.3:c.2760+20C>T
NG_050579.1:g.22906C>T
More... 		02/28/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIK3CG
Accession:XM_017012328
Location:INTRON

Gene Symbol:PIK3CG
Accession:XM_005250443
Location:INTRON

Gene Symbol:PIK3CG
Accession:XM_047420481
Location:INTRON

Gene Symbol:PIK3CG
Accession:NM_002649
Location:INTRON

Gene Symbol:PIK3CG
Accession:XM_047420479
Location:INTRON

Gene Symbol:PIK3CG
Accession:XM_011516316
Location:INTRON

Gene Symbol:PIK3CG
Accession:NM_001282426
Location:INTRON

Gene Symbol:PIK3CG
Accession:XM_047420480
Location:INTRON

Gene Symbol:PIK3CG
Accession:XM_011516317
Location:INTRON

Gene Symbol:PIK3CG
Accession:NM_001282427
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001810644 CLINVAR
dbSNP (RS) rs200932463 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIK3CG CLINVAR
OMIM 601232 CLINVAR