Variant #0001002197 (NC_000016.9:g.29818506C>T, NM_145239.2:c.-5204C>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.29818506C>T
DNA change (hg38) -
Published as MAZ(NM_002383.3):c.400C>T (p.(Pro134Ser))
ISCN -
DB-ID PRRT2_000066
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF22 NM_007317.2 ?/. - c.*1875C>T r.(=) p.(=)
PRRT2 NM_145239.2 ?/. - c.-5204C>T r.(?) p.(=)


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