RGD:13436066 Rat Genome Database

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Variant: RGD:13436066 -  Homo sapiens

RGD ID: 13436066
RS ID: rs184771174
ClinVar ID: CV433845
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127457201  PLOD3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 100,860,220
GRCh38 7 101,216,939
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012148.1:g.5792T>C
NC_000007.14:g.101216939A>G
NC_000007.13:g.100860220A>G
NM_001084.5:c.110-153T>C
 08/18/2016 intron variant benign AllHighlyPenetrant

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000506505 CLINVAR
dbSNP (RS) rs184771174 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PLOD3 CLINVAR
OMIM 603066 CLINVAR