RGD:8580082 Rat Genome Database

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Variant: RGD:8580082 -  Homo sapiens

RGD ID: 8580082
ClinVar ID: CV114487
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADAMTS3  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 73,202,573
GRCh38 4 72,336,856
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.72336856C>A
NC_000004.11:g.73202573C>A
NM_014243.2:c.861+2638G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ADAMTS3
Accession:NM_014243
Location:INTRON

Gene Symbol:ADAMTS3
Accession:XM_011532422
Location:INTRON

Gene Symbol:ADAMTS3
Accession:XM_011532421
Location:INTRON

Variant Samples