RGD:14728241 Rat Genome Database

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Variant: RGD:14728241 -  Homo sapiens

RGD ID: 14728241
RS ID: rs76718163
ClinVar ID: CV659612
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 145,878,621
GRCh38 3 146,160,834
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_182943.3:c.109+47G>C
NG_009251.1:g.5662G>C
NC_000003.12:g.146160834C>G
NC_000003.11:g.145878621C>G
More... 		06/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PLOD2
Accession:NM_182943
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448319
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448320
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_017006625
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_000935
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000834690 CLINVAR
dbSNP (RS) rs76718163 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR