Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28280 | A01 | 17326195 | C | T | upstream_gene_variant | MODIFIER | c.-4604C>T| |
S113 |
2 | BAA01g28280 | A01 | 17326577 | G | A | upstream_gene_variant | MODIFIER | c.-4222G>A| |
S246 S284 |
3 | BAA01g28280 | A01 | 17327032 | G | A | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S114 |
4 | BAA01g28280 | A01 | 17327110 | C | A | upstream_gene_variant | MODIFIER | c.-3689C>A| |
S37 |
5 | BAA01g28280 | A01 | 17327419 | G | A | upstream_gene_variant | MODIFIER | c.-3380G>A| |
S278 |
6 | BAA01g28280 | A01 | 17328322 | G | A | upstream_gene_variant | MODIFIER | c.-2477G>A| |
S45 |
7 | BAA01g28280 | A01 | 17329488 | C | T | upstream_gene_variant | MODIFIER | c.-1311C>T| |
S179 |
8 | BAA01g28280 | A01 | 17330836 | C | T | missense_variant | MODERATE | c.38C>T|p.Pro13Leu |
S136 |
9 | BAA01g28280 | A01 | 17330980 | G | A | missense_variant | MODERATE | c.182G>A|p.Gly61Asp |
S178 |
10 | BAA01g28280 | A01 | 17331117 | C | T | synonymous_variant | LOW | c.319C>T|p.Leu107Leu |
S78 |
11 | BAA01g28280 | A01 | 17331533 | G | A | intron_variant | MODIFIER | c.649+9G>A| |
S232 |
12 | BAA01g28280 | A01 | 17331586 | G | A | intron_variant | MODIFIER | c.650-44G>A| |
S23 |
13 | BAA01g28280 | A01 | 17332572 | G | A | synonymous_variant | LOW | c.1302G>A|p.Gly434Gly |
S122 |
14 | BAA01g28280 | A01 | 17332637 | C | T | missense_variant | MODERATE | c.1367C>T|p.Ser456Phe |
S286 |
15 | BAA01g28280 | A01 | 17333688 | G | A | downstream_gene_variant | MODIFIER | c.*690G>A| |
S244 |
16 | BAA01g28280 | A01 | 17334076 | C | T | downstream_gene_variant | MODIFIER | c.*1078C>T| |
S103 |
17 | BAA01g28280 | A01 | 17334145 | G | A | downstream_gene_variant | MODIFIER | c.*1147G>A| |
S288 |