RGD:8627689 Rat Genome Database

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Variant: RGD:8627689 -  Homo sapiens

RGD ID: 8627689
ClinVar ID: CV82833
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLN6  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 68,506,545
GRCh38 15 68,214,207
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.8:g.66293599G>A
NM_017882.2:c.297+83C>T
NG_008764.2:g.48005C>T
NC_000015.10:g.68214207G>A
More... 		intron|intron variant not provided Malignant melanoma, somatic

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