RGD:38468769 Rat Genome Database

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Variant: RGD:38468769 -  Homo sapiens

RGD ID: 38468769
RS ID: rs777653128
ClinVar ID: CV960431
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SZT2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 43,907,929
GRCh38 1 43,442,258
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.43442258C>A
NC_000001.10:g.43907929C>A
NM_015284.3:c.7703-10C>A
NM_015284.4:c.7703-10C>A
More... 		07/17/2023 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 RCV001246633 CLINVAR
dbSNP (RS) rs777653128 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SZT2 CLINVAR
OMIM 615463 CLINVAR