RGD:14722763 Rat Genome Database

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Variant: RGD:14722763 -  Homo sapiens

RGD ID: 14722763
RS ID: rs117909641
ClinVar ID: CV665911
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTMR2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 95,571,591
GRCh38 11 95,838,427
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_016156.6:c.1480-220G>A
NM_001243571.2:c.1264-220G>A
NM_201278.3:c.1264-220G>A
NM_201281.3:c.1264-220G>A
More... 		06/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MTMR2
Accession:NM_201278
Location:INTRON

Gene Symbol:MTMR2
Accession:XM_047427805
Location:INTRON

Gene Symbol:MTMR2
Accession:XM_047427806
Location:INTRON

Gene Symbol:MTMR2
Accession:NM_001243571
Location:INTRON

Gene Symbol:MTMR2
Accession:XM_047427807
Location:INTRON

Gene Symbol:MTMR2
Accession:NM_016156
Location:INTRON

Gene Symbol:MTMR2
Accession:XM_047427808
Location:INTRON

Gene Symbol:MTMR2
Accession:NM_201281
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832240 CLINVAR
dbSNP (RS) rs117909641 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTMR2 CLINVAR
OMIM 603557 CLINVAR