rs529107045 Rat Genome Database

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Variant: rs529107045 -  Homo sapiens

RGD ID: 150443707
RS ID: rs529107045
ClinVar ID: CV1264632
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: LOC127406595  MTO1  
Reference Nucleotide: -
Variant Nucleotide: AG
Position
Assembly Chr Position
GRCh37 6 74,172,074
GRCh38 6 73,462,351
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001123226.2:c.217+280_217+281insGA
NM_012123.4:c.217+280_217+281insGA
NM_133645.3:c.217+280_217+281insGA
NG_032856.2:g.5621_5622insGA
More... 		06/25/2018 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001679616 CLINVAR
dbSNP (RS) rs529107045 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTO1 CLINVAR
OMIM 614667 CLINVAR