Variant #0000333681 (NC_000023.10:g.36368166G>A, CXorf22(NM_152632.3):c.*360513G>A)

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.36368166G>A
DNA change (hg38) g.36350051G>A
Published as CXorf30(NM_001098843.4):c.955G>A (p.(Asp319Asn))
ISCN -
DB-ID CXorf30_000003
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) 0.00502 View details
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     
CXorf30 NM_001098843.4 ?/. - c.955G>A r.(?) p.(Asp319Asn)
CXorf59 NM_001304548.1 ?/. - c.8617G>A r.(?) p.(Asp2873Asn)
CXorf22 NM_152632.3 ?/. - c.*360513G>A r.(=) p.(=)