RGD:150468306 Rat Genome Database

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Variant: RGD:150468306 -  Homo sapiens

RGD ID: 150468306
RS ID: rs742034
ClinVar ID: CV1267918
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTSA  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 44,522,005
GRCh38 20 45,893,366
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000308.4:c.692+55A>G
NG_033108.1:g.2922T>C
NG_008291.1:g.7415A>G
NC_000020.11:g.45893366A>G
More... 		06/28/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CTSA
Accession:NM_001127695
Location:INTRON

Gene Symbol:CTSA
Accession:NM_000308
Location:INTRON

Gene Symbol:CTSA
Accession:NM_001167594
Location:INTRON

Gene Symbol:CTSA
Accession:NR_133656
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001694781 CLINVAR
dbSNP (RS) rs742034 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTSA CLINVAR
OMIM 613111 CLINVAR