RGD:11647180 Rat Genome Database

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Variant: RGD:11647180 -  Homo sapiens

RGD ID: 11647180
ClinVar ID: CV345993
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL9A3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 61,468,629
GRCh38 20 62,837,277
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016353.1:g.25216A>G
NC_000020.11:g.62837277A>G
NC_000020.10:g.61468629A>G
NM_001853.3:c.1786+12A>G
More... 		06/14/2016 intron variant uncertain significance

Variant Details
Variant Transcripts
Gene Symbol:COL9A3
Accession:XM_047439894
Location:INTRON

Gene Symbol:COL9A3
Accession:XM_047439895
Location:INTRON

Gene Symbol:COL9A3
Accession:NM_001853
Location:INTRON

Gene Symbol:COL9A3
Accession:XM_047439893
Location:INTRON

Gene Symbol:COL9A3
Accession:XM_017027666
Location:INTRON

Variant Samples