RGD:11650851 Rat Genome Database

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Variant: RGD:11650851 -  Homo sapiens

RGD ID: 11650851
RS ID: rs886059853
ClinVar ID: CV295096
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LMNB1  LOC127403726  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 126,112,513
GRCh38 5 126,776,821
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008360.2:g.4681G>A
NC_000005.10:g.126776821G>A
NC_000005.9:g.126112513G>A
NR_134488.1:n.199G>A
More... 		06/14/2016 2kb upstream variant|non-coding transcript variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:LMNB1
Accession:NR_134488
Location:EXON;NON-CODING

Gene Symbol:LMNB1
Accession:NM_005573
Location:INTRON

Gene Symbol:LMNB1
Accession:XM_047417174
Location:INTRON

Gene Symbol:LMNB1
Accession:NM_001198557
Location:INTRON

Gene Symbol:LMNB1
Accession:XM_047417173
Location:INTRON

Gene Symbol:LMNB1
Accession:XM_047417175
Location:INTRON

Gene Symbol:LMNB1
Accession:NR_177109
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000295564 CLINVAR
dbSNP (RS) rs886059853 CLINVAR
MedGen CN239186 CLINVAR
NCBI Gene LMNB1 CLINVAR
OMIM 150340 CLINVAR