Variant #0000615928 (NC_000016.9:g.29825852_29825853del, NC_000016.9(NM_145239.2):c.1012+66_1012+67del (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.29825852_29825853del
DNA change (hg38) g.29814531_29814532del
Published as PRRT2(NM_001256442.1):c.1078_1079delCC (p.P360Cfs*34)
ISCN -
DB-ID MVP_000013
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.*4300_*4301del r.(=) p.(=)
MVP NM_005115.4 +/. - c.-6015_-6014del r.(?) p.(=)
PAGR1 NM_024516.3 +/. - c.-1995_-1994del r.(?) p.(=)
PRRT2 NM_145239.2 +/. - c.1012+66_1012+67del r.(=) p.(=)


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