rs6148118 Rat Genome Database

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Variant: rs6148118 -  Homo sapiens

RGD ID: 14746498
RS ID: rs6148118
ClinVar ID: CV659585
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: PLOD2  
Reference Nucleotide: -
Variant Nucleotide: GCTAAACTAATTTA
Position
Assembly Chr Position
GRCh37 3 145,794,325
GRCh38 3 146,076,538
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1614+243_1614+244insTAAATTAGTTTAGC
NM_182943.3:c.1677+243_1677+244insTAAATTAGTTTAGC
NG_009251.1:g.89957_89958insTAAATTAGTTTAGC
NC_000003.12:g.146076538_146076539insGCTAAACTAATTTA
More... 		06/19/2018 intron variant benign none provided

Gene Symbol:PLOD2
Accession:XM_047448320
Location:3UTRS;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 RCV000844517 CLINVAR
dbSNP (RS) rs6148118 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR