rs35274473 Rat Genome Database

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Variant: rs35274473 -  Homo sapiens

RGD ID: 14709195
RS ID: rs35274473
ClinVar ID: CV659716
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: PLOD2  
Reference Nucleotide: TTTA
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 3 145,794,778 - 145,794,782
GRCh38 3 146,076,991 - 146,076,995
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000003.12:g.146076990_146076993del
NM_182943.2:c.1564-98_1564-95delTAAA
NM_000935.3:c.1501-98_1501-95del
NM_182943.3:c.1564-98_1564-95del
More... 		06/14/2018 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV000834259 CLINVAR
dbSNP (RS) rs35274473 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR