RGD:401905656 Rat Genome Database

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Variant: RGD:401905656 -  Homo sapiens

RGD ID: 401905656
ClinVar ID: CV2813683
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: MRE11  
Reference Nucleotide: -
Variant Nucleotide: GAGG
Position
Assembly Chr Position
GRCh37 11 94,152,628
GRCh38 11 94,419,462
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_85t1:c.*657_*660dup
NM_001330347.2:c.*660_*663dup
NM_005590.4:c.*660_*663dup
NM_005591.4:c.*660_*663dup
More... 		04/01/2023 3 prime utr variant benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

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Database
Acc Id
Source(s)
ClinVar RCV003396020 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MRE11 CLINVAR
OMIM 600814 CLINVAR