Variant #0000335068 (NC_000023.10:g.105912555T>C, NM_018015.5:c.2432T>C (CXorf57))

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.105912555T>C
DNA change (hg38) g.106669325T>C
Published as CXorf57(NM_001184782.1):c.2141T>C (p.(Val714Ala)), RADX(NM_018015.5):c.2432T>C (p.V811A)
ISCN -
DB-ID CXorf57_000007 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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf57 NM_018015.5 ?/. - c.2432T>C r.(?) p.(Val811Ala)


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