Genomic variant #0000334553

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70320588G>A
DNA change (hg38) -
Published as FOXO4(NM_001170931.1):c.343G>A (p.(Glu115Lys), p.(Glu170Lys))
ISCN -
DB-ID FOXO4_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
CXorf65 NM_001025265.2 ?/. - c.*3249C>T VUS r.(=) p.(=)
FOXO4 NM_005938.3 ?/. - c.508G>A VUS r.(?) p.(Glu170Lys)