Variant #0000681854 (NC_000022.10:g.32162660_32162661del, NC_000022.10(NM_001242896.1):c.363+6_363+7del (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.32162660_32162661del
DNA change (hg38) -
Published as DEPDC5(NM_001242896.2):c.363+6_363+7delAT, DEPDC5(NM_001242896.3):c.363+6_363+7del, DEPDC5(NM_001242896.3):c.363+6_363+7delAT
ISCN -
DB-ID DEPDC5_000159 See all 3 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) 0.00045 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.363+6_363+7del r.(=) p.(=)


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