Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27140 | A01 | 15516788 | G | A | upstream_gene_variant | MODIFIER | c.-1466G>A| |
S163 |
2 | BAA01g27140 | A01 | 15516790 | G | A | upstream_gene_variant | MODIFIER | c.-1464G>A| |
S181 |
3 | BAA01g27140 | A01 | 15517194 | C | T | upstream_gene_variant | MODIFIER | c.-1060C>T| |
S270 |
4 | BAA01g27140 | A01 | 15517431 | C | T | upstream_gene_variant | MODIFIER | c.-823C>T| |
S176 |
5 | BAA01g27140 | A01 | 15517581 | C | T | upstream_gene_variant | MODIFIER | c.-673C>T| |
S77 S82 |
6 | BAA01g27140 | A01 | 15517904 | G | A | upstream_gene_variant | MODIFIER | c.-350G>A| |
S288 |
7 | BAA01g27140 | A01 | 15518182 | C | T | upstream_gene_variant | MODIFIER | c.-72C>T| |
S233 |
8 | BAA01g27140 | A01 | 15518196 | G | A | upstream_gene_variant | MODIFIER | c.-58G>A| |
S157 |
9 | BAA01g27140 | A01 | 15518536 | C | T | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S200 |
10 | BAA01g27140 | A01 | 15519323 | T | C | missense_variant | MODERATE | c.535T>C|p.Phe179Leu |
|
11 | BAA01g27140 | A01 | 15520486 | G | A | synonymous_variant | LOW | c.1302G>A|p.Ser434Ser |
S198 |
12 | BAA01g27140 | A01 | 15520812 | C | T | missense_variant | MODERATE | c.1628C>T|p.Pro543Leu |
S177 |
13 | BAA01g27140 | A01 | 15522262 | G | A | downstream_gene_variant | MODIFIER | c.*1437G>A| |
S83 S88 |
14 | BAA01g27140 | A01 | 15523569 | C | T | downstream_gene_variant | MODIFIER | c.*2744C>T| |
S11 |
15 | BAA01g27140 | A01 | 15523592 | C | T | downstream_gene_variant | MODIFIER | c.*2767C>T| |
S90 |
16 | BAA01g27140 | A01 | 15524560 | G | A | downstream_gene_variant | MODIFIER | c.*3735G>A| |
S265 |
17 | BAA01g27140 | A01 | 15524712 | G | A | downstream_gene_variant | MODIFIER | c.*3887G>A| |
S94 |