RGD:8586301 Rat Genome Database

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Variant: RGD:8586301 -  Homo sapiens

RGD ID: 8586301
ClinVar ID: CV120900
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SIRPG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 1,656,642
GRCh38 20 1,675,996
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000020.11:g.1675996C>T
NC_000020.10:g.1656642C>T
 uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SIRPG
Accession:XM_011529286
Location:5UTRS;INTRON

Gene Symbol:SIRPG
Accession:NM_080816
Location:INTRON

Gene Symbol:SIRPG
Accession:NM_018556
Location:INTRON

Gene Symbol:SIRPG
Accession:XM_011529287
Location:INTRON

Gene Symbol:SIRPG
Accession:NM_001039508
Location:INTRON

Gene Symbol:SIRPG
Accession:XM_005260749
Location:INTRON

Variant Samples