RGD:150495001 Rat Genome Database

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Variant: RGD:150495001 -  Homo sapiens

RGD ID: 150495001
RS ID: rs138769157
ClinVar ID: CV1204928
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACADM  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 76,211,898
GRCh38 1 75,746,213
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.75746213G>T
NC_000001.10:g.76211898G>T
NM_001286042.2:c.600+299G>T
NM_000016.6:c.708+299G>T
More... 		08/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACADM
Accession:NM_000016
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001127328
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286042
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286044
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286043
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001593420 CLINVAR
dbSNP (RS) rs138769157 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACADM CLINVAR
OMIM 607008 CLINVAR