RGD:8651149 Rat Genome Database

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Variant: RGD:8651149 -  Homo sapiens

RGD ID: 8651149
ClinVar ID: CV127724
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOCAD  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 20,746,633
GRCh38 9 20,746,634
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.20746634G>T
NC_000009.11:g.20746633G>T
NM_017794.4:c.392+6294G>T
 intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:FOCAD
Accession:NM_001375567
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423539
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423534
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423533
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_017014856
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423536
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423531
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423532
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_017014859
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_024447586
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_017014855
Location:INTRON

Gene Symbol:FOCAD
Accession:NM_001375570
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423540
Location:INTRON

Gene Symbol:FOCAD
Accession:NM_017794
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_017014852
Location:INTRON

Gene Symbol:FOCAD
Accession:NM_001375568
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423537
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423538
Location:INTRON

Gene Symbol:FOCAD
Accession:XM_047423535
Location:INTRON

Variant Samples