RGD:8651216 Rat Genome Database

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Variant: RGD:8651216 -  Homo sapiens

RGD ID: 8651216
ClinVar ID: CV127791
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LINGO2  LOC105376003  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 28,649,593
GRCh38 9 28,649,595
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.28649595T>G
NC_000009.11:g.28649593T>G
NM_001258282.1:c.-314+20605A>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LINGO2
Accession:NM_152570
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:NM_001258282
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_017014303
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:NM_001354574
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:NM_001354575
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422814
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422810
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422812
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422818
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422815
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422811
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422813
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422816
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_047422817
Location:5UTRS;INTRON

Gene Symbol:LINGO2
Accession:XM_011517724
Location:INTRON

Gene Symbol:LINGO2
Accession:XM_011517728
Location:INTRON

Gene Symbol:LINGO2
Accession:XM_017014305
Location:INTRON

Gene Symbol:LINGO2
Accession:XM_017014304
Location:INTRON

Gene Symbol:LINGO2
Accession:XM_017014306
Location:INTRON

Gene Symbol:LINGO2
Accession:XM_017014307
Location:INTRON

Gene Symbol:LOC105376003
Accession:XR_929533
Location:INTRON;NON-CODING

Variant Samples