RGD:150423482 Rat Genome Database

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Variant: RGD:150423482 -  Homo sapiens

RGD ID: 150423482
RS ID: rs866000561
ClinVar ID: CV1182963
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACADM  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 76,215,397
GRCh38 1 75,749,712
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.282+153C>T
NM_001286042.2:c.741+153C>T
NM_000016.6:c.849+153C>T
NM_001127328.3:c.861+153C>T
More... 		08/06/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
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

Gene Symbol:ACADM
Accession:NM_001286044
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001555381 CLINVAR
dbSNP (RS) rs866000561 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACADM CLINVAR
OMIM 607008 CLINVAR