Variant #0000982379 (NC_000017.10:g.26898177_26898179del, NM_033198.3:c.67_69del (PIGS))

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.26898177_26898179del
DNA change (hg38) -
Published as PIGS(NM_033198.4):c.67_69del (p.(Phe23del))
ISCN -
DB-ID ALDOC_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) 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDOC NM_005165.2 ?/. - c.*2370_*2372del r.(=) p.(=)
PIGS NM_033198.3 ?/. - c.67_69del r.(?) p.(Phe23del)


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