Variant #0000728977 (NC_000023.10:g.48925324C>T, NM_007213.1:c.*4204G>A (PRAF2))

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.48925324C>T
DNA change (hg38) -
Published as CCDC120(NM_001271836.1):c.1569C>T (p.A523=)
ISCN -
DB-ID CCDC120_000022
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) 1.0E-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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRAF2 NM_007213.1 -?/. - c.*4204G>A r.(=) p.(=)
CCDC120 NM_033626.2 -?/. - c.1569C>T r.(?) p.(Ala523=)


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