Variant #0000335838 (NC_000023.10:g.148628489C>A, NM_178124.4:c.458C>A (CXorf40A))

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.148628489C>A
DNA change (hg38) g.149546943C>A
Published as CXorf40A(NM_001171907.2):c.458C>A (p.(Pro153Gln))
ISCN -
DB-ID CXorf40A_000023
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) 0.00161 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 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf40A NM_001171907.1 -?/. - c.458C>A r.(?) p.(Pro153His)
CXorf40A NM_178124.4 -?/. - c.458C>A r.(?) p.(Pro153His)


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