RGD:8650119 Rat Genome Database

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Variant: RGD:8650119 -  Homo sapiens

RGD ID: 8650119
ClinVar ID: CV126693
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL22A1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 139,646,621
GRCh38 8 138,634,378
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.138634378T>G
NC_000008.10:g.139646621T>G
NM_152888.2:c.3609+632A>C
NM_152888.1:c.3609+632A>C
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:COL22A1
Accession:XM_011516888
Location:3UTRS;EXON

Gene Symbol:COL22A1
Accession:XM_047421412
Location:3UTRS;EXON

Gene Symbol:COL22A1
Accession:NM_152888
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_011516886
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_011516884
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_011516885
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_011516883
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_011516887
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_011516889
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_017013151
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_017013150
Location:INTRON

Gene Symbol:COL22A1
Accession:XM_017013152
Location:INTRON

Gene Symbol:COL22A1
Accession:XR_001745487
Location:INTRON;NON-CODING

Variant Samples