Variant #0000272742 (NC_000023.10:g.48925232G>A, NM_007213.1:c.*4296C>T (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.48925232G>A
DNA change (hg38) g.49067696G>A
Published as CCDC120(NM_001271836.1):c.1477G>A (p.A493T)
ISCN -
DB-ID CCDC120_000010
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) 0.0001 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRAF2 NM_007213.1 ?/. - c.*4296C>T r.(=) p.(=)
CCDC120 NM_033626.2 ?/. - c.1477G>A r.(?) p.(Ala493Thr)


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