RGD:150460111 Rat Genome Database

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Variant: RGD:150460111 -  Homo sapiens

RGD ID: 150460111
RS ID: rs72881978
ClinVar ID: CV1203471
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SZT2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 43,869,683
GRCh38 1 43,404,012
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.327+238C>T
NM_001365999.1:c.327+238C>T
NG_029091.1:g.19128C>T
NC_000001.11:g.43404012C>T
More... 		09/18/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SZT2
Accession:NM_001365999
Location:INTRON

Gene Symbol:SZT2
Accession:NM_015284
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001586678 CLINVAR
dbSNP (RS) rs72881978 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SZT2 CLINVAR
OMIM 615463 CLINVAR