Variant #0000047995 (NC_000017.10:g.(10700001_16000000)_(16000001_22200000)del)

Individual ID 00025123
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(10700001_16000000)_(16000001_22200000)del
DNA change (hg38) -
Published as del17p12-p11.2
ISCN -
DB-ID chr17_001476
Variant remarks cells from patient had significantly reduced levels of the two GPI anchor markers, CD59 and a GPI-binding toxin, aerolysin (FLAER)
Reference PubMed: Ng 2012
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Philippe Campeau
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Philippe Campeau
Date created 2014-12-04 23:33:42 +01:00 (CET)
Date last edited 2019-03-03 17:42:23 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000025126 DNA SEQ-NG - - PIGL 1 Philippe Campeau


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