RGD:15132664 Rat Genome Database

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Variant: RGD:15132664 -  Homo sapiens

RGD ID: 15132664
RS ID: rs1577033146
ClinVar ID: CV759229
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIK3CB  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 138,375,125
GRCh38 3 138,656,283
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006219.3:c.2943-9C>T
NC_000003.11:g.138375125G>A
NC_000003.12:g.138656283G>A
NM_006219.2:c.2943-9C>T
More... 		04/04/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIK3CB
Accession:NM_006219
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448310
Location:INTRON

Gene Symbol:PIK3CB
Accession:NM_001256045
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448314
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_011512895
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448315
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448313
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_017006619
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448312
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448308
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448307
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_006713659
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448311
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448309
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000920381 CLINVAR
dbSNP (RS) rs1577033146 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene PIK3CB CLINVAR
OMIM 602925 CLINVAR