RGD:8586845 Rat Genome Database

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Variant: RGD:8586845 -  Homo sapiens

RGD ID: 8586845
ClinVar ID: CV121468
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIAA1671  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 25,497,281
GRCh38 22 25,101,314
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000022.11:g.25101314C>T
NC_000022.10:g.25497281C>T
NM_001145206.1:c.4530+51950C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KIAA1671
Accession:NM_001386932
Location:INTRON

Gene Symbol:KIAA1671
Accession:XM_006724346
Location:INTRON

Gene Symbol:KIAA1671
Accession:NM_001386933
Location:INTRON

Gene Symbol:KIAA1671
Accession:XM_047441557
Location:INTRON

Gene Symbol:KIAA1671
Accession:NM_001386930
Location:INTRON

Gene Symbol:KIAA1671
Accession:NM_001386934
Location:INTRON

Gene Symbol:KIAA1671
Accession:NM_001145206
Location:INTRON

Gene Symbol:KIAA1671
Accession:XM_047441556
Location:INTRON

Gene Symbol:KIAA1671
Accession:NM_001386935
Location:INTRON

Variant Samples