Variant #0000333678 (NC_000023.10:g.36162895A>G, CXorf22(NM_152632.3):c.*155242A>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.36162895A>G
DNA change (hg38) g.36144778A>G
Published as CHDC2(NM_173695.2):c.1478A>G (p.(His493Arg))
ISCN -
DB-ID CXorf59_000013
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) 0.00037 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf30 NM_001098843.4 ?/. - c.-84695A>G r.(?) p.(=)
CXorf59 NM_001304548.1 ?/. - c.5536-441A>G r.(=) p.(=)
CXorf22 NM_152632.3 ?/. - c.*155242A>G r.(=) p.(=)