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
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
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

Variant Details
Variant Samples

Additional Information

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