RGD:407503771 Rat Genome Database

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Variant: RGD:407503771 -  Homo sapiens

RGD ID: 407503771
ClinVar ID: CV3446795
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MGST2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 140,624,647
GRCh38 4 139,703,493
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001204368.2:c.197C>T
NM_001204366.2:c.268C>T
NM_002413.5:c.268C>T
NM_001204367.2:c.64C>T
More... 		06/07/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004645582 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MGST2 CLINVAR
OMIM 601733 CLINVAR