Variant #0000710807 (NC_000012.11:g.(90486683_90488249)_(90490259_90492571)del)

Individual ID 00324548
Chromosome 12
Allele Both (homozygous)
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.(90486683_90488249)_(90490259_90492571)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr12_007219
Variant remarks <26kb deletion incl. rs12817868 and rs10858953
Reference PubMed: Durlu 2014
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-01-05 14:58:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000325740 DNA SEQ Blood - POC1B 2 Najlae Akhiyate


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