RGD:401925142 Rat Genome Database

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Variant: RGD:401925142 -  Homo sapiens

RGD ID: 401925142
ClinVar ID: CV2805268
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 145,806,358
GRCh38 3 146,088,571
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1005+15A>G
NM_182943.3:c.1005+15A>G
NG_009251.1:g.77925A>G
NC_000003.12:g.146088571T>C
More... 		10/17/2023 intron variant likely benign AllHighlyPenetrant

Gene Symbol:PLOD2
Accession:XM_047448320
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_000935
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_182943
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_017006625
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448319
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV003405089 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR