Variant #0000557822 (NC_000016.9:g.29825640C>T, NC_000016.9(NM_145239.2):c.880-14C>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.29825640C>T
DNA change (hg38) g.29814319C>T
Published as PRRT2(NM_145239.2):c.880-14C>T
ISCN -
DB-ID MVP_000008
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) 0.00072 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 -?/. - c.*4088C>T r.(=) p.(=)
MVP NM_005115.4 -?/. - c.-6227C>T r.(?) p.(=)
PAGR1 NM_024516.3 -?/. - c.-2207C>T r.(?) p.(=)
PRRT2 NM_145239.2 -?/. - c.880-14C>T r.(=) p.(=)


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