Variant #0000571789 (NC_000022.10:g.32193632G>A, NM_001242896.1:c.814G>A (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.32193632G>A
DNA change (hg38) g.31797646G>A
Published as DEPDC5(NM_001242896.2):c.814G>A (p.V272I), DEPDC5(NM_001242896.3):c.814G>A (p.V272I)
ISCN -
DB-ID DEPDC5_000004 See all 4 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) 0.00227 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 2019-07-18 18:22:55 +02:00 (CEST)
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.814G>A r.(?) p.(Val272Ile)


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