RGD:156353985 Rat Genome Database

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Variant: RGD:156353985 -  Homo sapiens

RGD ID: 156353985
ClinVar ID: CV1880036
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DGAT1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 145,541,750
GRCh38 8 144,318,087
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.751+8C>G
NG_034192.1:g.13833C>G
NC_000008.11:g.144318087G>C
NC_000008.10:g.145541750G>C
 05/23/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DGAT1
Accession:NM_012079
Location:INTRON

Gene Symbol:DGAT1
Accession:XM_011517356
Location:INTRON

Gene Symbol:DGAT1
Accession:XM_047422387
Location:INTRON

Gene Symbol:DGAT1
Accession:XM_047422389
Location:INTRON

Gene Symbol:DGAT1
Accession:XM_047422388
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003065090 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DGAT1 CLINVAR
OMIM 604900 CLINVAR