RGD:150516725 Rat Genome Database

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Variant: RGD:150516725 -  Homo sapiens

RGD ID: 150516725
RS ID: rs4403552
ClinVar ID: CV1227209
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STS  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 7,243,304
GRCh38 X 7,325,263
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000351.7:c.1082-76G>A
NM_001320752.2:c.1082-76G>A
NM_001320753.2:c.1082-76G>A
NM_001320754.2:c.1082-76G>A
More... 		08/20/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:STS
Accession:NM_001320750
Location:INTRON

Gene Symbol:STS
Accession:NM_001320753
Location:INTRON

Gene Symbol:STS
Accession:NM_001320751
Location:INTRON

Gene Symbol:STS
Accession:NM_001320752
Location:INTRON

Gene Symbol:STS
Accession:XM_047442107
Location:INTRON

Gene Symbol:STS
Accession:NM_001320754
Location:INTRON

Gene Symbol:STS
Accession:NM_000351
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001639307 CLINVAR
dbSNP (RS) rs4403552 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene STS CLINVAR
OMIM 300747 CLINVAR