Variant #0000880728 (NC_000006.11:g.(?_100054862)_(100062667_?)dup)

Individual ID 00419091
Chromosome 6
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_100054862)_(100062667_?)dup
DNA change (hg38) -
Published as 100054862-100062667dup
ISCN -
DB-ID PRDM13_000029 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jun Xiao
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Jun Xiao
Date created 2022-10-17 07:43:57 +02:00 (CEST)
Date last edited 2023-03-20 17:10:34 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000420390 DNA PCRq blood WGS PRDM13 1 Jun Xiao


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