RGD:14727634 Rat Genome Database

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Variant: RGD:14727634 -  Homo sapiens

RGD ID: 14727634
ClinVar ID: CV671576
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL9A3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 61,464,440
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000020.11:g.62833088G>A
NC_000020.10:g.61464440G>A
NM_001853.3:c.1368+24G>A
06/16/2018 benign

Variant Details
Variant Transcripts
Gene Symbol:COL9A3
Accession:NM_001853
Location:INTRON

Variant Samples