Variant #0001026689 (NC_000016.9:g.29821438_29821452dup, NM_145239.2:c.-2272_-2258dup (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.29821438_29821452dup
DNA change (hg38) -
Published as MAZ(NM_002383.4):c.1320_1334dupGGCGGCAGCGGCAGC (p.A444_A448dup)
ISCN -
DB-ID PRRT2_000068
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF22 NM_007317.2 -?/. - c.*4807_*4821dup r.(=) p.(=)
PRRT2 NM_145239.2 -?/. - c.-2272_-2258dup r.(?) p.(=)


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