RGD:14744647 Rat Genome Database

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Variant: RGD:14744647 -  Homo sapiens

RGD ID: 14744647
RS ID: rs7548695
ClinVar ID: CV657980
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACADM  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 76,198,033
GRCh38 1 75,732,348
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.131-296A>G
NG_007045.2:g.12991A>G
NC_000001.11:g.75732348A>G
NC_000001.10:g.76198033A>G
More... 		06/19/2018 intron variant benign none provided

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

Gene Symbol:ACADM
Accession:NM_001286042
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001127328
Location:INTRON

Gene Symbol:ACADM
Accession:NM_001286043
Location:INTRON

Gene Symbol:ACADM
Accession:NM_000016
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000842888 CLINVAR
dbSNP (RS) rs7548695 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ACADM CLINVAR
OMIM 607008 CLINVAR