RGD:13796631 Rat Genome Database

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Variant: RGD:13796631 -  Homo sapiens

RGD ID: 13796631
RS ID: rs41277720
ClinVar ID: CV552863
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAP2K1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 66,773,975
GRCh38 15 66,481,637
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_725:g.99765G>A
LRG_725t1:c.569-118G>A
NC_000015.9:g.66773975G>A
NM_002755.4:c.569-118G>A
More... 		06/15/2018 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:NM_001411065
Location:INTRON

Gene Symbol:MAP2K1
Accession:NM_002755
Location:INTRON

Gene Symbol:MAP2K1
Accession:XM_017022411
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000680674 CLINVAR
dbSNP (RS) rs41277720 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MAP2K1 CLINVAR
OMIM 176872 CLINVAR