RGD:150491273 Rat Genome Database

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Variant: RGD:150491273 -  Homo sapiens

RGD ID: 150491273
RS ID: rs2298307
ClinVar ID: CV1222729
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127406672  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 80,816,296
GRCh38 6 80,106,579
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_009775.2:g.4953T>C
NC_000006.12:g.80106579T>C
NC_000006.11:g.80816296T>C
 03/03/2015 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001618791 CLINVAR
dbSNP (RS) rs2298307 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BCKDHB CLINVAR
OMIM 248611 CLINVAR