RGD:13786689 Rat Genome Database

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Variant: RGD:13786689 -  Homo sapiens

RGD ID: 13786689
RS ID: rs2077056
ClinVar ID: CV549812
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTSA  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 44,526,979
GRCh38 20 45,898,340
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008291.1:g.12389C>T
NC_000020.11:g.45898340C>T
NC_000020.10:g.44526979C>T
NM_000308.2:c.1414-27C>T
More... 		07/15/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CTSA
Accession:NM_001167594
Location:INTRON

Gene Symbol:CTSA
Accession:NM_001127695
Location:INTRON

Gene Symbol:CTSA
Accession:NM_000308
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000675501 CLINVAR
dbSNP (RS) rs2077056 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTSA CLINVAR
OMIM 613111 CLINVAR