RGD:8636338 Rat Genome Database

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Variant: RGD:8636338 -  Homo sapiens

RGD ID: 8636338
ClinVar ID: CV91561
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD300LD-AS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 17 72,588,676
GRCh38 17 74,592,537
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000017.9:g.70100271G>A
NM_152460.2:c.491G>A
NC_000017.11:g.74592537G>A
NC_000017.10:g.72588676G>A
More... 		missense|missense variant|2kb upstream variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:CD300LD-AS1
Accession:NR_171004
Location:EXON;NON-CODING

Gene Symbol:CD300LD-AS1
Accession:NR_171003
Location:EXON;NON-CODING

Variant Samples