RGD:10397214 Rat Genome Database

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Variant: RGD:10397214 -  Homo sapiens

RGD ID: 10397214
ClinVar ID: CV202882
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: CLN6  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 15 68,506,613
GRCh38 15 68,214,275
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_017882.2:c.297+15del
NM_017882.2:c.297+15delC
NG_008764.2:g.47937delC
NC_000015.10:g.68214275delG
More... 		09/06/2013 intron variant benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:CLN6
Accession:NM_017882
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CLN6
Accession:NM_001411068
Location:INTRON

Variant Samples