Variant #0001006020 (NC_000022.10:g.32150851G>C, NM_001242896.1:c.-57G>C (DEPDC5))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32150851G>C
DNA change (hg38) -
Published as DEPDC5(NM_001242896.1):c.-57G>C (p.?)
ISCN -
DB-ID DEPDC5_000001 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DEPDC5 NM_001242896.1 ?/. - c.-57G>C r.(?) p.(=)
PRR14L NM_173566.2 ?/. - c.-4924C>G r.(?) p.(=)


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