RGD:407494543 Rat Genome Database

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Variant: RGD:407494543 -  Homo sapiens

RGD ID: 407494543
ClinVar ID: CV3456809
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAPK8IP1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 45,924,103
GRCh38 11 45,902,552
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005456.4:c.785C>T
NG_012153.1:g.21902C>T
NC_000011.10:g.45902552C>T
NC_000011.9:g.45924103C>T
More... 		04/17/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004643015 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MAPK8IP1 CLINVAR
OMIM 604641 CLINVAR