rs80102622 Rat Genome Database

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Variant: rs80102622 -  Homo sapiens

RGD ID: 14729640
RS ID: rs80102622
ClinVar ID: CV662339
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTO1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 74,176,381
GRCh38 6 73,466,658
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001123226.2:c.535+52G>A
NM_012123.4:c.535+52G>A
NM_133645.3:c.535+52G>A
NG_032856.2:g.9928G>A
More... 		06/14/2018 intron variant likely benign none provided

Gene Symbol:MTO1
Accession:NM_133645
Location:INTRON

Gene Symbol:MTO1
Accession:NM_001123226
Location:INTRON

Gene Symbol:MTO1
Accession:XM_047418606
Location:INTRON

Gene Symbol:MTO1
Accession:XM_047418607
Location:INTRON

Gene Symbol:MTO1
Accession:NM_012123
Location:INTRON

Gene Symbol:MTO1
Accession:XM_047418605
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000835315 CLINVAR
dbSNP (RS) rs80102622 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTO1 CLINVAR
OMIM 614667 CLINVAR