Variant #0000619646 (NC_000023.10:g.48924777C>T, NM_007213.1:c.*4751G>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.48924777C>T
DNA change (hg38) g.49067241C>T
Published as CCDC120(NM_001271836.1):c.1022C>T (p.A341V)
ISCN -
DB-ID PRAF2_000005
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) 5.0E-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 2019-12-04 15:24:38 +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.*4751G>A r.(=) p.(=)
CCDC120 NM_033626.2 -?/. - c.1022C>T r.(?) p.(Ala341Val)


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