Variant #0000867522 (NC_000023.10:g.70320697G>A, CXorf65(NM_001025265.2):c.*3140C>T)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.70320697G>A
DNA change (hg38) -
Published as FOXO4(NM_005938.3):c.617G>A (p.R206Q)
ISCN -
DB-ID FOXO4_000014
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf65 NM_001025265.2 ?/. - c.*3140C>T r.(=) p.(=)
FOXO4 NM_005938.3 ?/. - c.617G>A r.(?) p.(Arg206Gln)