Variant #0000324695 (NC_000016.9:g.29818533_29818538del, NM_145239.2:c.-5177_-5172del (PRRT2))

Chromosome 16
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.29818533_29818538del
DNA change (hg38) g.29807212_29807217del
Published as MAZ(NM_001042539.1):c.424_429del (p.(Ala144_Ala145del))
ISCN -
DB-ID MAZ_000004
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 ?/. - c.427_432del r.(?) p.(Pro143_Ala144del)
KIF22 NM_007317.2 ?/. - c.*1902_*1907del r.(=) p.(=)
PRRT2 NM_145239.2 ?/. - c.-5177_-5172del r.(?) p.(=)


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