RGD:15135801 Rat Genome Database

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Variant: RGD:15135801 -  Homo sapiens

RGD ID: 15135801
RS ID: rs774201583
ClinVar ID: CV786981
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTSK  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 150,771,636
GRCh38 1 150,799,160
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.150799160A>T
NC_000001.10:g.150771636A>T
NM_000396.4:c.890+8T>A
NG_011848.1:g.14177T>A
More... 		12/04/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CTSK
Accession:NM_000396
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000981993 CLINVAR
dbSNP (RS) rs774201583 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTSK CLINVAR
OMIM 601105 CLINVAR