RGD:8652869 Rat Genome Database

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Variant: RGD:8652869 -  Homo sapiens

RGD ID: 8652869
ClinVar ID: CV129444
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GAS2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 22,721,997
GRCh38 11 22,700,451
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.10:g.22700451G>A
NC_000011.9:g.22721997G>A
NM_001143830.1:c.267+14662G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GAS2
Accession:NM_001143830
Location:INTRON

Gene Symbol:GAS2
Accession:XM_047426749
Location:INTRON

Gene Symbol:GAS2
Accession:XM_047426746
Location:INTRON

Gene Symbol:GAS2
Accession:NM_005256
Location:INTRON

Gene Symbol:GAS2
Accession:XM_047426744
Location:INTRON

Gene Symbol:GAS2
Accession:NM_001391936
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:GAS2
Accession:XM_011519971
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:GAS2
Accession:XM_011519975
Location:INTRON

Gene Symbol:GAS2
Accession:XM_011519972
Location:INTRON

Gene Symbol:GAS2
Accession:NM_001351224
Location:INTRON

Gene Symbol:GAS2
Accession:NM_001391937
Location:INTRON

Gene Symbol:GAS2
Accession:NM_001391935
Location:INTRON

Gene Symbol:GAS2
Accession:XM_047426747
Location:INTRON

Gene Symbol:GAS2
Accession:NM_001391934
Location:INTRON

Gene Symbol:GAS2
Accession:XM_047426745
Location:INTRON

Gene Symbol:GAS2
Accession:NM_001391933
Location:INTRON

Gene Symbol:GAS2
Accession:NM_177553
Location:INTRON

Gene Symbol:GAS2
Accession:XM_047426750
Location:INTRON

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

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

Gene Symbol:GAS2
Accession:NR_147085
Location:INTRON;NON-CODING

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

Variant Samples