RGD:13476973 Rat Genome Database

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Variant: RGD:13476973 -  Homo sapiens

RGD ID: 13476973
RS ID: rs1555951288
ClinVar ID: CV446667
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAOA  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 43,603,039
GRCh38 X 43,743,792
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000023.10:g.43603039A>G
NM_000240.2:c.1263-2A>G
NG_008957.2:g.92632A>G
NC_000023.11:g.43743792A>G
More... 		08/10/2017 splice acceptor variant pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:MAOA
Accession:NM_001270458
Location:INTRON

Gene Symbol:MAOA
Accession:NM_000240
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000520275 CLINVAR
dbSNP (RS) rs1555951288 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene MAOA CLINVAR
OMIM 309850 CLINVAR