RGD:401830598 Rat Genome Database

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Variant: RGD:401830598 -  Homo sapiens

RGD ID: 401830598
ClinVar ID: CV2743282
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACADM  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 76,216,135
GRCh38 1 75,750,450
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001127328.3:c.862-1G>A
NG_007045.2:g.31093G>A
NM_001286044.2:c.283-1G>A
NC_000001.11:g.75750450G>A
More... 		splice acceptor variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:ACADM
Accession:NM_001127328
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286043
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286044
Location:INTRON

Gene Symbol:ACADM
Accession:NM_000016
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286042
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003326109 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ACADM CLINVAR
OMIM 607008 CLINVAR