Variant #0000856660 (NC_000023.10:g.48925259C>T, NM_007213.1:c.*4269G>A (PRAF2))

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.48925259C>T
DNA change (hg38) -
Published as CCDC120(NM_001163321.4):c.1609C>T (p.(Arg537Cys)), CCDC120(NM_001163322.2):c.1468C>T (p.R490C)
ISCN -
DB-ID CCDC120_000029 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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRAF2 NM_007213.1 ?/. - c.*4269G>A r.(=) p.(=)
CCDC120 NM_033626.2 ?/. - c.1504C>T r.(?) p.(Arg502Cys)


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