RGD:13539636 Rat Genome Database

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Variant: RGD:13539636 -  Homo sapiens

RGD ID: 13539636
RS ID: rs754129486
ClinVar ID: CV505140
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLN6  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 68,500,768
GRCh38 15 68,208,430
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008764.2:g.53782C>T
NC_000015.10:g.68208430G>A
NC_000015.9:g.68500768G>A
NM_017882.2:c.666-20C>T
More... 		06/30/2017 intron variant likely benign AllHighlyPenetrant

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

Gene Symbol:CLN6
Accession:NM_017882
Location:INTRON

Gene Symbol:CLN6
Accession:NM_001411068
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000613547 CLINVAR
dbSNP (RS) rs754129486 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CLN6 CLINVAR
OMIM 606725 CLINVAR