RGD:14740305 Rat Genome Database

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Variant: RGD:14740305 -  Homo sapiens

RGD ID: 14740305
RS ID: rs12983789
ClinVar ID: CV670293
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127891597  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 41,903,421
GRCh38 19 41,397,516
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_013004.1:g.4728A>T
NC_000019.10:g.41397516A>T
NC_000019.9:g.41903421A>T
NM_000709.3:c.-312A>T
More... 		06/19/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000840286 CLINVAR
dbSNP (RS) rs12983789 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BCKDHA CLINVAR
OMIM 608348 CLINVAR