RGD:15130400 Rat Genome Database

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Variant: RGD:15130400 -  Homo sapiens

RGD ID: 15130400
RS ID: rs764300040
ClinVar ID: CV775105
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MSH3  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 79,968,186
GRCh38 5 80,672,367
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000005.9:g.79968186T>G
NC_000005.10:g.80672367T>G
NC_000005.9:g.79968186T>G
NM_002439.4:c.909+7T>G
More... 		07/26/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MSH3
Accession:NM_002439
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000942045 CLINVAR
dbSNP (RS) rs764300040 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MSH3 CLINVAR
OMIM 600887 CLINVAR