Variant #0000270770 (NC_000022.10:g.32150985del, NC_000022.10(NM_001242896.1):c.58+20del (DEPDC5))

Chromosome 22
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.32150985del
DNA change (hg38) g.31754999del
Published as DEPDC5(NM_001242896.3):c.58+20delT
ISCN -
DB-ID DEPDC5_000021
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DEPDC5 NM_001242896.1 -?/. - c.58+20del r.(=) p.(=)
PRR14L NM_173566.2 -?/. - c.-5056del r.(?) p.(=)


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