RGD:150472697 Rat Genome Database

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Variant: RGD:150472697 -  Homo sapiens

RGD ID: 150472697
RS ID: rs1146572
ClinVar ID: CV1252287
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACADM  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 76,194,306
GRCh38 1 75,728,621
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001286044.2:c.-268+3804A>G
NM_001286042.2:c.10+3804A>G
NM_000016.6:c.118+133A>G
NM_001286043.2:c.118+133A>G
More... 		03/03/2015 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACADM
Accession:NM_001286044
Location:5UTRS;INTRON

Gene Symbol:ACADM
Accession:NM_001127328
Location:INTRON

Gene Symbol:ACADM
Accession:NM_000016
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286043
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286042
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001671488 CLINVAR
dbSNP (RS) rs1146572 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACADM CLINVAR
OMIM 607008 CLINVAR