Variant #0000810325 (NC_000023.10:g.36011366A>G, CXorf22(NM_152632.3):c.*3713A>G)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36011366A>G
DNA change (hg38) -
Published as CFAP47(NM_001304548.1):c.3027A>G (p.P1009=)
ISCN -
DB-ID CXorf22_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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf30 NM_001098843.4 -?/. - c.-236224A>G r.(?) p.(=)
CXorf59 NM_001304548.1 -?/. - c.3027A>G r.(?) p.(Pro1009=)
CXorf22 NM_152632.3 -?/. - c.*3713A>G r.(=) p.(=)