RGD:8579659 Rat Genome Database

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Variant: RGD:8579659 -  Homo sapiens

RGD ID: 8579659
ClinVar ID: CV114061
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZFYVE28  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 2,404,479
GRCh38 4 2,402,752
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.2402752A>T
NC_000004.11:g.2404479A>T
NM_001172656.1:c.39+15533T>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ZFYVE28
Accession:NM_001172659
Location:INTRON

Gene Symbol:ZFYVE28
Accession:NM_001172660
Location:INTRON

Gene Symbol:ZFYVE28
Accession:NM_001172658
Location:INTRON

Gene Symbol:ZFYVE28
Accession:NM_001172656
Location:INTRON

Gene Symbol:ZFYVE28
Accession:NM_001172657
Location:INTRON

Gene Symbol:ZFYVE28
Accession:NM_020972
Location:INTRON

Variant Samples