Variant #0000615927 (NC_000016.9:g.29824955G>A, NM_145239.2:c.580G>A (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.29824955G>A
DNA change (hg38) g.29813634G>A
Published as PRRT2(NM_001256443.2):c.580G>A (p.E194K)
ISCN -
DB-ID MVP_000012
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) 6.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.*3403G>A r.(=) p.(=)
MVP NM_005115.4 ?/. - c.-6912G>A r.(?) p.(=)
PAGR1 NM_024516.3 ?/. - c.-2892G>A r.(?) p.(=)
PRRT2 NM_145239.2 ?/. - c.580G>A r.(?) p.(Glu194Lys)


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