RGD:8650020 Rat Genome Database

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Variant: RGD:8650020 -  Homo sapiens

RGD ID: 8650020
ClinVar ID: CV126594
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KHDRBS3  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 136,508,282
GRCh38 8 135,496,039
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.135496039C>A
NC_000008.10:g.136508282C>A
NM_006558.2:c.89-25198C>A
NM_006558.1:c.89-25198C>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KHDRBS3
Accession:XM_011516799
Location:INTRON

Gene Symbol:KHDRBS3
Accession:NM_006558
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_005250758
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_011516798
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_011516797
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_047421268
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_024447052
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_005250757
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XM_047421269
Location:INTRON

Gene Symbol:KHDRBS3
Accession:XR_928287
Location:INTRON;NON-CODING

Gene Symbol:KHDRBS3
Accession:XR_242372
Location:INTRON;NON-CODING

Gene Symbol:KHDRBS3
Accession:XR_001745458
Location:INTRON;NON-CODING

Gene Symbol:KHDRBS3
Accession:XR_001745455
Location:INTRON;NON-CODING

Gene Symbol:KHDRBS3
Accession:XR_001745457
Location:INTRON;NON-CODING

Gene Symbol:KHDRBS3
Accession:XR_001745456
Location:INTRON;NON-CODING

Variant Samples