Genomic variant #0000287863

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.70321314G>A
DNA change (hg38) -
Published as FOXO4(NM_005938.3):c.1234G>A (p.V412I)
ISCN -
DB-ID FOXO4_000007
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_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf65 NM_001025265.2 -?/. - c.*2523C>T r.(=) p.(=)
FOXO4 NM_005938.3 -?/. - c.1234G>A r.(?) p.(Val412Ile)