Variant #0000557817 (NC_000016.9:g.29825024del, NM_145239.2:c.649del (PRRT2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29825024del
DNA change (hg38) g.29813703del
Published as PRRT2(NM_001256443.2):c.649delC (p.R217Efs*12), PRRT2(NM_145239.2):c.649delC (p.R217Efs*12)
ISCN -
DB-ID PRRT2_000032 See all 2 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 +/. - c.*3472del r.(?) p.(=)
MVP NM_005115.4 +/. - c.-6843del r.(?) p.(=)
PAGR1 NM_024516.3 +/. - c.-2823del r.(?) p.(=)
PRRT2 NM_145239.2 +/. - c.649del r.(?) p.(Arg217GlufsTer12)


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