RGD:8579465 Rat Genome Database

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Variant: RGD:8579465 -  Homo sapiens

RGD ID: 8579465
ClinVar ID: CV113866
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LCORL  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 17,950,845
GRCh38 4 17,949,222
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_153686.7:c.430+12681A>G
NG_015822.1:g.77639A>G
NC_000004.12:g.17949222T>C
NC_000004.11:g.17950845T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LCORL
Accession:NM_001365658
Location:5UTRS;INTRON

Gene Symbol:LCORL
Accession:NM_001365659
Location:5UTRS;INTRON

Gene Symbol:LCORL
Accession:NM_001166139
Location:INTRON

Gene Symbol:LCORL
Accession:NM_001365660
Location:INTRON

Gene Symbol:LCORL
Accession:NM_001365665
Location:INTRON

Gene Symbol:LCORL
Accession:XM_017007965
Location:INTRON

Gene Symbol:LCORL
Accession:NM_153686
Location:INTRON

Gene Symbol:LCORL
Accession:NM_001365663
Location:INTRON

Gene Symbol:LCORL
Accession:NM_001365662
Location:INTRON

Gene Symbol:LCORL
Accession:NM_001365661
Location:INTRON

Gene Symbol:LCORL
Accession:NM_001394446
Location:INTRON

Gene Symbol:LCORL
Accession:XM_047449965
Location:INTRON

Gene Symbol:LCORL
Accession:XM_047449966
Location:INTRON

Gene Symbol:LCORL
Accession:NR_158566
Location:INTRON;NON-CODING

Gene Symbol:LCORL
Accession:NR_158565
Location:INTRON;NON-CODING

Gene Symbol:LCORL
Accession:NR_158563
Location:INTRON;NON-CODING

Gene Symbol:LCORL
Accession:NR_158564
Location:INTRON;NON-CODING

Gene Symbol:LCORL
Accession:NR_136669
Location:INTRON;NON-CODING

Gene Symbol:LCORL
Accession:NR_158567
Location:INTRON;NON-CODING

Gene Symbol:LCORL
Accession:NR_158568
Location:INTRON;NON-CODING

Variant Samples