RGD:150407781 Rat Genome Database

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Variant: RGD:150407781 -  Homo sapiens

RGD ID: 150407781
RS ID: rs139763113
ClinVar ID: CV1192874
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SZT2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 43,890,994
GRCh38 1 43,425,323
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001365999.1:c.2645+116G>C
NM_015284.4:c.2645+116G>C
NC_000001.11:g.43425323G>C
NG_029091.1:g.40439G>C
More... 		08/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SZT2
Accession:NM_015284
Location:INTRON

Gene Symbol:SZT2
Accession:NM_001365999
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001572437 CLINVAR
dbSNP (RS) rs139763113 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SZT2 CLINVAR
OMIM 615463 CLINVAR