RGD:15181238 Rat Genome Database

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Variant: RGD:15181238 -  Homo sapiens

RGD ID: 15181238
RS ID: rs192283718
ClinVar ID: CV744009
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIK3CB  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 138,433,300
GRCh38 3 138,714,458
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.1302+10T>C
NC_000003.12:g.138714458A>G
NC_000003.11:g.138433300A>G
NM_006219.2:c.1302+10T>C
 02/22/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIK3CB
Accession:XM_047448314
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448309
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_006713659
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448315
Location:INTRON

Gene Symbol:PIK3CB
Accession:NM_001256045
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_017006619
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448311
Location:INTRON

Gene Symbol:PIK3CB
Accession:NM_006219
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_011512895
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448310
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448312
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448313
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448307
Location:INTRON

Gene Symbol:PIK3CB
Accession:XM_047448308
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000907537 CLINVAR
dbSNP (RS) rs192283718 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIK3CB CLINVAR
OMIM 602925 CLINVAR