Variant #0000333380 (NC_000023.10:g.19971119T>C, CXorf23(NM_198279.3):c.1616A>G)

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.19971119T>C
DNA change (hg38) g.19953001T>C
Published as CXorf23(NM_198279.3):c.1616A>G (p.(Tyr539Cys))
ISCN -
DB-ID CXorf23_000002
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     
CXorf23 NM_198279.3 ?/. - c.1616A>G r.(?) p.(Tyr539Cys)