rs41263844 Rat Genome Database

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Variant: rs41263844 -  Homo sapiens

RGD ID: 150333655
RS ID: rs41263844
ClinVar ID: CV1169522
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL2A1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 48,377,957
GRCh38 12 47,984,174
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.25329G>A
NC_000012.12:g.47984174C>T
NC_000012.11:g.48377957C>T
NM_033150.3:c.1681-34G>A
More... 		06/26/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:COL2A1
Accession:NM_001844
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018829
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018830
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018828
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_017018831
Location:INTRON

Gene Symbol:COL2A1
Accession:XM_047428315
Location:INTRON

Gene Symbol:COL2A1
Accession:NM_033150
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001537441 CLINVAR
dbSNP (RS) rs41263844 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL2A1 CLINVAR
OMIM 120140 CLINVAR