RGD:8652676 Rat Genome Database

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Variant: RGD:8652676 -  Homo sapiens

RGD ID: 8652676
ClinVar ID: CV129251
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIRREL3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 126,482,637
GRCh38 11 126,612,742
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032531.3:c.56-49830G>C
NG_012971.1:g.393130G>C
NC_000011.10:g.126612742C>G
NC_000011.9:g.126482637C>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KIRREL3
Accession:XM_011543032
Location:INTRON

Gene Symbol:KIRREL3
Accession:XM_017018419
Location:INTRON

Gene Symbol:KIRREL3
Accession:XM_011543027
Location:INTRON

Gene Symbol:KIRREL3
Accession:XM_047427715
Location:INTRON

Gene Symbol:KIRREL3
Accession:XM_011543030
Location:INTRON

Gene Symbol:KIRREL3
Accession:NM_001301097
Location:INTRON

Gene Symbol:KIRREL3
Accession:XM_011543026
Location:INTRON

Gene Symbol:KIRREL3
Accession:NM_032531
Location:INTRON

Gene Symbol:KIRREL3
Accession:NM_001161707
Location:INTRON

Variant Samples