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
|
|