RGD:8651254 Rat Genome Database

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Variant: RGD:8651254 -  Homo sapiens

RGD ID: 8651254
ClinVar ID: CV127829
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PHF24  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 34,867,491
GRCh38 9 34,867,494
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000009.12:g.34867494G>C
NC_000009.11:g.34867491G>C
 uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:PHF24
Accession:XM_017014555
Location:5UTRS;INTRON

Gene Symbol:PHF24
Accession:XM_017014553
Location:5UTRS;INTRON

Gene Symbol:PHF24
Accession:XM_017014556
Location:5UTRS;INTRON

Gene Symbol:PHF24
Accession:XM_017014554
Location:5UTRS;INTRON

Gene Symbol:PHF24
Accession:NM_001395370
Location:INTRON

Gene Symbol:PHF24
Accession:XM_047423103
Location:INTRON

Gene Symbol:PHF24
Accession:NM_001395371
Location:INTRON

Gene Symbol:PHF24
Accession:NM_001395372
Location:INTRON

Gene Symbol:PHF24
Accession:XM_047423102
Location:INTRON

Gene Symbol:PHF24
Accession:NM_001347982
Location:INTRON

Gene Symbol:PHF24
Accession:NM_015297
Location:INTRON

Gene Symbol:PHF24
Accession:NM_001304333
Location:INTRON

Gene Symbol:PHF24
Accession:NM_001347983
Location:INTRON

Gene Symbol:PHF24
Accession:NM_001395369
Location:INTRON

Gene Symbol:PHF24
Accession:NR_136307
Location:INTRON;NON-CODING

Gene Symbol:PHF24
Accession:NR_136308
Location:INTRON;NON-CODING

Variant Samples