Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40330 | A01 | 26755857 | C | T | upstream_gene_variant | MODIFIER | c.-1700C>T| |
S77 S82 |
2 | BAA01g40330 | A01 | 26755922 | G | A | upstream_gene_variant | MODIFIER | c.-1635G>A| |
S201 |
3 | BAA01g40330 | A01 | 26755940 | C | T | upstream_gene_variant | MODIFIER | c.-1617C>T| |
S161 |
4 | BAA01g40330 | A01 | 26757020 | C | T | upstream_gene_variant | MODIFIER | c.-537C>T| |
S88 |
5 | BAA01g40330 | A01 | 26757591 | C | T | missense_variant | MODERATE | c.35C>T|p.Pro12Leu |
S256 |
6 | BAA01g40330 | A01 | 26758163 | G | A | missense_variant | MODERATE | c.607G>A|p.Glu203Lys |
S126 |
7 | BAA01g40330 | A01 | 26758662 | C | T | missense_variant | MODERATE | c.1106C>T|p.Thr369Ile |
S192 |
8 | BAA01g40330 | A01 | 26758771 | G | A | stop_gained | HIGH | c.1215G>A|p.Trp405* |
S204 |
9 | BAA01g40330 | A01 | 26759008 | C | T | synonymous_variant | LOW | c.1452C>T|p.Phe484Phe |
S59 |
10 | BAA01g40330 | A01 | 26759102 | G | A | missense_variant | MODERATE | c.1546G>A|p.Ala516Thr |
S149 |
11 | BAA01g40330 | A01 | 26759763 | C | T | missense_variant | MODERATE | c.2207C>T|p.Ala736Val |
S292 |
12 | BAA01g40330 | A01 | 26760357 | G | A | missense_variant | MODERATE | c.2652G>A|p.Met884Ile |
S296 |
13 | BAA01g40330 | A01 | 26760766 | C | T | missense_variant | MODERATE | c.2984C>T|p.Ser995Phe |
S78 S83 |
14 | BAA01g40330 | A01 | 26761728 | G | A | missense_variant | MODERATE | c.3644G>A|p.Ser1215Asn |
S114 |
15 | BAA01g40330 | A01 | 26761830 | G | A | missense_variant | MODERATE | c.3746G>A|p.Gly1249Glu |
S126 |