Variant #0000001118 (NC_000016.9:g.226799G>T)

Individual ID 00000236, 00000996, 00001305, 00001337, 00001489, 00001567
Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.226799G>T
Reference Yao et al
DB-ID chr16_000068
Frequency -
Variant remarks Codon28(G>T)
ClassClinical Uncertain significance
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     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000235 DNA SEQ-NG-I BCL11A, HBA2, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 35 Qi Ming
0000000995 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2 51 Qi Ming
0000001304 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2 51 Qi Ming
0000001336 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2 51 Qi Ming
0000001488 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 49 Qi Ming
0000001566 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2 51 Qi Ming