RGD:152131700 Rat Genome Database

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Variant: RGD:152131700 -  Homo sapiens

RGD ID: 152131700
RS ID: rs780570738
ClinVar ID: CV1660328
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD3  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 100,853,455
GRCh38 7 101,210,174
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001084.5:c.1615-13C>A
NG_012148.1:g.12557C>A
NC_000007.14:g.101210174G>T
NC_000007.13:g.100853455G>T
 06/01/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PLOD3
Accession:NM_001084
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002176885 CLINVAR
dbSNP (RS) rs780570738 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD3 CLINVAR
OMIM 603066 CLINVAR