Variant #0000557804 (NC_000016.9:g.29818615C>T, NM_145239.2:c.-5095C>T (PRRT2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.29818615C>T
DNA change (hg38) g.29807294C>T
Published as MAZ(NM_001042539.1):c.509C>T (p.(Thr170Met))
ISCN -
DB-ID PRRT2_000051
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 2019-07-18 18:22:55 +02:00 (CEST)
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.509C>T r.(?) p.(Thr170Met)
KIF22 NM_007317.2 -?/. - c.*1984C>T r.(=) p.(=)
PRRT2 NM_145239.2 -?/. - c.-5095C>T r.(?) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.