Variant #0000148357 (NC_000011.9:g.(121200001_130800000)_qterdel)

Individual ID 00019483
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(121200001_130800000)_qterdel
DNA change (hg38) -
Published as -
ISCN 11q24-11qter del
DB-ID chr11_000769
Variant remarks -
Reference PubMed: Huizing 2001
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-12-06 21:44:44 +01:00 (CET)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000019468 DNA SEQ - - HPS3 3 William (Bill) Oetting


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