RGD:405117175 Rat Genome Database

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Variant: RGD:405117175 -  Homo sapiens

RGD ID: 405117175
ClinVar ID: CV2961690
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DGAT1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 145,542,738
GRCh38 8 144,319,075
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_034192.1:g.12845C>G
NC_000008.11:g.144319075G>C
NC_000008.10:g.145542738G>C
NM_012079.6:c.289-7C>G
 05/19/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003671027 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DGAT1 CLINVAR
OMIM 604900 CLINVAR