Variant #0000573908 (NC_000023.10:g.139038830T>C, CXorf66(NM_001013403.2):c.311A>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.139038830T>C
DNA change (hg38) g.139956671T>C
Published as CXorf66(NM_001013403.2):c.311A>G (p.Q104R)
ISCN -
DB-ID CXorf66_000009
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf66 NM_001013403.2 -?/. - c.311A>G r.(?) p.(Gln104Arg)