Variant #0001055510 (NC_000016.9:g.29825657C>T, NM_145239.2:c.883C>T (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.29825657C>T
DNA change (hg38) -
Published as PRRT2(NM_145239.3):c.883C>T (p.(Arg295Trp))
ISCN -
DB-ID MVP_000029
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MVP NM_005115.4 ?/. - c.-6210C>T r.(?) p.(=)
PAGR1 NM_024516.3 ?/. - c.-2190C>T r.(?) p.(=)
PRRT2 NM_145239.2 ?/. - c.883C>T r.(?) p.(Arg295Trp)


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