Variant #0000335713 (NC_000023.10:g.139047624G>A, CXorf66(NM_001013403.2):c.32C>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.139047624G>A
DNA change (hg38) g.139965465G>A
Published as CXorf66(NM_001013403.2):c.32C>T (p.(Ser11Phe))
ISCN -
DB-ID CXorf66_000006
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf66 NM_001013403.2 ?/. - c.32C>T r.(?) p.(Ser11Phe)