Variant #0000001131 (NC_000016.9:g.97115_175257del)

Individual ID 00001972
Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.97115_175257del
Reference Shang et al
DB-ID HBA1_000002 See all 2 reported entries
Frequency -
Variant remarks -a78
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Technique     

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Variants found     

Owner     
0000001971 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2 50 Qi Ming