rs1469695989 Rat Genome Database

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Variant: rs1469695989 -  Homo sapiens

RGD ID: 127233134
RS ID: rs1469695989
ClinVar ID: CV1079412
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL2A1  LOC105369752  LOC127824065  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 48,375,188
GRCh38 12 47,981,405
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008072.1:g.28098C>T
NC_000012.12:g.47981405G>A
NC_000012.11:g.48375188G>A
NM_033150.3:c.2203-9C>T
More... 		07/19/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LOC105369752
Accession:XR_944910
Location:EXON;NON-CODING

Gene Symbol:COL2A1
Accession:XM_017018830
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018831
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_047428315
Location:INTRON

Gene Symbol:COL2A1
Accession:NM_001844
Location:INTRON

Gene Symbol:COL2A1
Accession:NM_033150
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018829
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018828
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001396004 CLINVAR
dbSNP (RS) rs1469695989 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL2A1 CLINVAR
OMIM 120140 CLINVAR