RGD:26905007 Rat Genome Database

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Variant: RGD:26905007 -  Homo sapiens

RGD ID: 26905007
RS ID: rs1743352039
ClinVar ID: CV851998
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MSH3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 80,024,664
GRCh38 5 80,728,845
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002439.5:c.1454-6T>A
NG_016607.2:g.79371T>A
NC_000005.10:g.80728845T>A
NC_000005.9:g.80024664T>A
More... 		01/29/2024 intron variant likely benign|uncertain significance 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 RCV001071423 CLINVAR
dbSNP (RS) rs1743352039 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MSH3 CLINVAR
OMIM 600887 CLINVAR