Variant #0000557809 (NC_000016.9:g.29824442G>A, NM_145239.2:c.67G>A (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.29824442G>A
DNA change (hg38) g.29813121G>A
Published as PRRT2(NM_001256443.1):c.67G>A (p.E23K), PRRT2(NM_001256443.2):c.67G>A (p.E23K), PRRT2(NM_145239.2):c.67G>A (p.E23K)
ISCN -
DB-ID PRRT2_000025 See all 3 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) 0.00108 View details
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 -?/. - c.*2890G>A r.(=) p.(=)
MVP NM_005115.4 -?/. - c.-7425G>A r.(?) p.(=)
PAGR1 NM_024516.3 -?/. - c.-3405G>A r.(?) p.(=)
PRRT2 NM_145239.2 -?/. - c.67G>A r.(?) p.(Glu23Lys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.