Variant #0000514577 (NC_000002.11:g.219209686_219209691del, NM_001077399.2:c.*72201_*72206del (PNKD))

Chromosome 2
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.219209686_219209691del
DNA change (hg38) g.218344963_218344968del
Published as PNKD(NM_015488.4):c.1140_1145delTATGCA (p.M381_H382del), PNKD(NM_015488.5):c.1140_1145delTATGCA (p.M381_H382del)
ISCN -
DB-ID PNKD_000013 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNKD NM_001077399.2 -?/. - c.*72201_*72206del r.(=) p.(=)
TMBIM1 NM_022152.4 -?/. - c.-52542_-52537del r.(?) p.(=)


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