RGD:597635561 Rat Genome Database

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Variant: RGD:597635561 -  Homo sapiens

RGD ID: 597635561
ClinVar ID: CV3697404
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAPK8IP1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 45,926,371
GRCh38 11 45,904,820
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005456.4:c.1879T>G
NG_012153.1:g.24170T>G
NC_000011.10:g.45904820T>G
NC_000011.9:g.45926371T>G
More... 		11/10/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004940642 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MAPK8IP1 CLINVAR
OMIM 604641 CLINVAR