RGD:150499011 Rat Genome Database

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Variant: RGD:150499011 -  Homo sapiens

RGD ID: 150499011
RS ID: rs74113509
ClinVar ID: CV1254289
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AMPD1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 115,229,161
GRCh38 1 114,686,540
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001172626.2:c.369+205A>G
NM_000036.3:c.381+205A>G
NG_008012.1:g.14016A>G
NC_000001.11:g.114686540T>C
More... 		06/18/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:AMPD1
Accession:NM_000036
Location:INTRON

Gene Symbol:AMPD1
Accession:NM_001172626
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676463 CLINVAR
dbSNP (RS) rs74113509 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AMPD1 CLINVAR
OMIM 102770 CLINVAR