RGD:15120627 Rat Genome Database

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Variant: RGD:15120627 -  Homo sapiens

RGD ID: 15120627
RS ID: rs146228551
ClinVar ID: CV780197
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BICRA  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 48,185,419
GRCh38 19 47,682,162
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015711.3:c.2283+10C>T
NC_000019.10:g.47682162C>T
NC_000019.9:g.48185419C>T
NM_001394372.1:c.2283+10C>T
 10/24/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BICRA
Accession:NM_015711
Location:INTRON

Gene Symbol:BICRA
Accession:NM_001394372
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000962751 CLINVAR
dbSNP (RS) rs146228551 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BICRA CLINVAR
OMIM 605690 CLINVAR