rs876658165 Rat Genome Database

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Variant: rs876658165 -  Homo sapiens

RGD ID: 11089279
RS ID: rs876658165
ClinVar ID: CV234460
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MRE11  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 94,169,065
GRCh38 11 94,435,899
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Age of Onset
Trait Synonyms
NM_005590.4:c.1843G>T
NP_001317276.1:p.Val642Leu
LRG_85t1:c.1927G>T
LRG_85:g.62976G>T
More... 		05/12/2024 missense variant uncertain significance adult Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV234460HumanHereditary Neoplastic Syndromes  IAGP 8554872ClinVar Annotator: match by term: Hereditary cancer-predisposing syndromeClinVar 
Gene Symbol:MRE11
Accession:NM_005591
Location:INTRON

Gene Symbol:MRE11
Accession:XM_047426967
Location:INTRON

Gene Symbol:MRE11
Accession:NM_005590
Location:INTRON

Gene Symbol:MRE11
Accession:XM_011542837
Location:INTRON

Gene Symbol:MRE11
Accession:XM_017017772
Location:INTRON

Gene Symbol:MRE11
Accession:NM_001330347
Location:INTRON

Gene Symbol:MRE11
Accession:XM_006718842
Location:INTRON

Gene Symbol:MRE11
Accession:XM_005274008
Location:INTRON

Gene Symbol:MRE11
Accession:XM_047426968
Location:INTRON

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

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

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

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

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Database
Acc Id
Source(s)
ClinVar RCV000214612 CLINVAR
dbSNP (RS) rs876658165 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene MRE11A CLINVAR
OMIM 600814 CLINVAR
SNOMED CT 699346009 CLINVAR