RGD:13797469 Rat Genome Database

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Variant: RGD:13797469 -  Homo sapiens

RGD ID: 13797469
RS ID: rs112381615
ClinVar ID: CV552860
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAP2K1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 66,736,683
GRCh38 15 66,444,345
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008305.1:g.62473C>A
LRG_725t1:c.517-311C>A
LRG_725:g.62473C>A
NM_002755.4:c.517-311C>A
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MAP2K1
Accession:XM_011521783
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MAP2K1
Accession:XM_017022411
Location:INTRON

Gene Symbol:MAP2K1
Accession:NM_001411065
Location:INTRON

Gene Symbol:MAP2K1
Accession:NM_002755
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000681244 CLINVAR
dbSNP (RS) rs112381615 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MAP2K1 CLINVAR
OMIM 176872 CLINVAR