Variant #0000557814 (NC_000016.9:g.29825019C>G, NM_145239.2:c.644C>G (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.29825019C>G
DNA change (hg38) g.29813698C>G
Published as PRRT2(NM_001256443.1):c.644C>G (p.P215R), PRRT2(NM_145239.2):c.644C>G (p.P215R)
ISCN -
DB-ID PRRT2_000010 See all 4 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) 0.00081 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 -?/. - c.*3467C>G r.(=) p.(=)
MVP NM_005115.4 -?/. - c.-6848C>G r.(?) p.(=)
PAGR1 NM_024516.3 -?/. - c.-2828C>G r.(?) p.(=)
PRRT2 NM_145239.2 -?/. - c.644C>G r.(?) p.(Pro215Arg)


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