Variant #0000981828 (NC_000016.9:g.29824375_29824376del, NM_145239.2:c.-1_1del (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.29824375_29824376del
DNA change (hg38) -
Published as PRRT2(NM_145239.3):c.-1_1del (p.(Met1?))
ISCN -
DB-ID MVP_000021
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MVP NM_005115.4 ?/. - c.-7492_-7491del r.(?) p.(=)
PAGR1 NM_024516.3 ?/. - c.-3472_-3471del r.(?) p.(=)
PRRT2 NM_145239.2 ?/. - c.-1_1del r.? p.?


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