RGD:14733179 Rat Genome Database

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Variant: RGD:14733179 -  Homo sapiens

RGD ID: 14733179
RS ID: rs59385667
ClinVar ID: CV667920
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLN6  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 68,510,693
GRCh38 15 68,218,355
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_017882.3:c.198+181A>G
NG_008764.2:g.43857A>G
NC_000015.10:g.68218355T>C
NC_000015.9:g.68510693T>C
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CLN6
Accession:NM_001411068
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CLN6
Accession:NM_017882
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000836983 CLINVAR
dbSNP (RS) rs59385667 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLN6 CLINVAR
OMIM 606725 CLINVAR