RGD:152152898 Rat Genome Database

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Variant: RGD:152152898 -  Homo sapiens

RGD ID: 152152898
RS ID: rs757124080
ClinVar ID: CV1545185
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SZT2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 43,903,063
GRCh38 1 43,437,392
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.6017-14T>C
NM_001365999.1:c.6188-14T>C
NG_029091.1:g.52508T>C
NC_000001.11:g.43437392T>C
More... 		10/10/2021 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 References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002139794 CLINVAR
dbSNP (RS) rs757124080 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SZT2 CLINVAR
OMIM 615463 CLINVAR