Variant #0000305531 (NC_000017.10:g.7139133_7139134del, NM_004422.2:c.-1553_-1552del (DVL2))

Chromosome 17
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.7139133_7139134del
DNA change (hg38) g.7235814_7235815del
Published as PHF23(NM_024297.3):c.1023_1024delAT (p.C342Lfs*13)
ISCN -
DB-ID PHF23_000001
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-11 15:36:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DVL2 NM_004422.2 ?/. - c.-1553_-1552del r.(?) p.(=)
GABARAP NM_007278.1 ?/. - c.*5039_*5040del r.(=) p.(=)
PHF23 NM_024297.2 ?/. - c.1023_1024del r.(?) p.(Cys342LeufsTer13)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.