Variant #0000693533 (NC_000023.10:g.23928481A>G, CXorf58(NM_152761.2):c.62A>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.23928481A>G
DNA change (hg38) -
Published as CXorf58(NM_001169574.1):c.62A>G (p.(Gln21Arg))
ISCN -
DB-ID CXorf58_000014 See all 2 reported entries
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) 0.00489 View details
Owner VKGL-NL_Leiden
Database submission license No license selected
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOO NM_024122.4 -?/. - c.-2662T>C r.(?) p.(=)
CXorf58 NM_152761.2 -?/. - c.62A>G r.(?) p.(Gln21Arg)