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 |

Variant on transcripts
Screenings
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