rs12281066 Rat Genome Database

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Variant: rs12281066 -  Homo sapiens

RGD ID: 150450851
RS ID: rs12281066
ClinVar ID: CV1205319
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MRE11  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 94,212,254
GRCh38 11 94,479,088
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001330347.2:c.403-212C>A
NM_005590.4:c.403-212C>A
NM_005591.4:c.403-212C>A
LRG_85:g.19787C>A
More... 		04/05/2019 intron variant likely benign none provided

Gene Symbol:MRE11
Accession:XM_005274008
Location:5UTRS;INTRON

Gene Symbol:MRE11
Accession:XM_017017772
Location:INTRON

Gene Symbol:MRE11
Accession:NM_005591
Location:INTRON

Gene Symbol:MRE11
Accession:XM_006718842
Location:INTRON

Gene Symbol:MRE11
Accession:NM_001330347
Location:INTRON

Gene Symbol:MRE11
Accession:XM_011542837
Location:INTRON

Gene Symbol:MRE11
Accession:XM_047426967
Location:INTRON

Gene Symbol:MRE11
Accession:NM_005590
Location:INTRON

Gene Symbol:MRE11
Accession:XM_047426968
Location:INTRON

Gene Symbol:MRE11
Accession:XR_007062482
Location:INTRON;NON-CODING

Gene Symbol:MRE11
Accession:XR_007062484
Location:INTRON;NON-CODING

Gene Symbol:MRE11
Accession:XR_007062483
Location:INTRON;NON-CODING

Gene Symbol:MRE11
Accession:XR_947828
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV001585219 CLINVAR
dbSNP (RS) rs12281066 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MRE11 CLINVAR
OMIM 600814 CLINVAR