RGD:150500057 Rat Genome Database

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Variant: RGD:150500057 -  Homo sapiens

RGD ID: 150500057
RS ID: rs1862162
ClinVar ID: CV1256024
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIK3R1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 67,584,758
GRCh38 5 68,288,930
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_453t1:c.917-3329A>G
NM_181524.2:c.16+179A>G
NM_181523.3:c.917-3329A>G
LRG_453:g.78175A>G
More... 		06/26/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIK3R1
Accession:XM_017009585
Location:INTRON

Gene Symbol:PIK3R1
Accession:NM_181524
Location:INTRON

Gene Symbol:PIK3R1
Accession:XM_005248542
Location:INTRON

Gene Symbol:PIK3R1
Accession:XM_047417316
Location:INTRON

Gene Symbol:PIK3R1
Accession:NM_181523
Location:INTRON

Gene Symbol:PIK3R1
Accession:NM_001242466
Location:INTRON

Gene Symbol:PIK3R1
Accession:NM_181504
Location:INTRON

Gene Symbol:PIK3R1
Accession:XM_047417315
Location:INTRON

Gene Symbol:PIK3R1
Accession:XM_047417317
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676647 CLINVAR
dbSNP (RS) rs1862162 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIK3R1 CLINVAR
OMIM 171833 CLINVAR