RGD:8652893 Rat Genome Database

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Variant: RGD:8652893 -  Homo sapiens

RGD ID: 8652893
ClinVar ID: CV129468
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LUZP2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 24,696,263
GRCh38 11 24,674,717
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001009909.3:c.63-54452A>T
NG_030588.1:g.182748A>T
NC_000011.10:g.24674717A>T
NC_000011.9:g.24696263A>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LUZP2
Accession:XM_017017648
Location:5UTRS;INTRON

Gene Symbol:LUZP2
Accession:XM_017017649
Location:5UTRS;INTRON

Gene Symbol:LUZP2
Accession:NM_001252008
Location:5UTRS;INTRON

Gene Symbol:LUZP2
Accession:XM_047426868
Location:INTRON

Gene Symbol:LUZP2
Accession:XM_047426869
Location:INTRON

Gene Symbol:LUZP2
Accession:NM_001252010
Location:INTRON

Gene Symbol:LUZP2
Accession:XM_047426871
Location:INTRON

Gene Symbol:LUZP2
Accession:NM_001009909
Location:INTRON

Gene Symbol:LUZP2
Accession:XM_047426870
Location:INTRON

Variant Samples