Variant #0000575754 (NC_000023.10:g.36064979C>T, NM_001304548.1:c.4016C>T (CXorf59))

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.36064979C>T
DNA change (hg38) g.36046862C>T
Published as CFAP47(NM_001304548.1):c.4016C>T (p.T1339I)
ISCN -
DB-ID CXorf59_000006
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXorf30 NM_001098843.4 -?/. - c.-182611C>T r.(?) p.(=)
CXorf59 NM_001304548.1 -?/. - c.4016C>T r.(?) p.(Thr1339Ile)
CXorf22 NM_152632.3 -?/. - c.*57326C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.