RGD:151830715 Rat Genome Database

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Variant: RGD:151830715 -  Homo sapiens

RGD ID: 151830715
RS ID: rs766480470
ClinVar ID: CV1516440
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SZT2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 43,907,819
GRCh38 1 43,442,148
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015284.4:c.7702+18G>T
NM_001365999.1:c.7873+18G>T
NG_029091.1:g.57264G>T
NC_000001.11:g.43442148G>T
More... 		07/05/2022 intron variant likely benign|uncertain significance 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 References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002030774 CLINVAR
dbSNP (RS) rs766480470 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SZT2 CLINVAR
OMIM 615463 CLINVAR