RGD:150480265 Rat Genome Database

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Variant: RGD:150480265 -  Homo sapiens

RGD ID: 150480265
RS ID: rs76350592
ClinVar ID: CV1282574
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SMARCB1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 24,133,786
GRCh38 22 23,791,599
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003073.5:c.94-157C>T
LRG_520:g.9637C>T
NG_009303.1:g.9637C>T
NC_000022.11:g.23791599C>T
More... 		06/23/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SMARCB1
Accession:NM_001362877
Location:INTRON

Gene Symbol:SMARCB1
Accession:NM_001007468
Location:INTRON

Gene Symbol:SMARCB1
Accession:NM_001317946
Location:INTRON

Gene Symbol:SMARCB1
Accession:NM_003073
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001714614 CLINVAR
dbSNP (RS) rs76350592 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SMARCB1 CLINVAR
OMIM 601607 CLINVAR