RGD:405188678 Rat Genome Database

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Variant: RGD:405188678 -  Homo sapiens

RGD ID: 405188678
ClinVar ID: CV3149488
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DGAT1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 145,541,364
GRCh38 8 144,317,701
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012079.6:c.906C>T
NG_034192.1:g.14219C>T
NC_000008.11:g.144317701G>A
NC_000008.10:g.145541364G>A
More... 		09/06/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003843214 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DGAT1 CLINVAR
OMIM 604900 CLINVAR