Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04170 | A09 | 2506253 | C | T | upstream_gene_variant | MODIFIER | c.-4782C>T| |
S212 |
2 | BAA09g04170 | A09 | 2506911 | G | A | upstream_gene_variant | MODIFIER | c.-4124G>A| |
S262 |
3 | BAA09g04170 | A09 | 2510844 | C | T | upstream_gene_variant | MODIFIER | c.-191C>T| |
S287 |
4 | BAA09g04170 | A09 | 2510851 | C | T | upstream_gene_variant | MODIFIER | c.-184C>T| |
S18 |
5 | BAA09g04170 | A09 | 2511353 | C | T | intron_variant | MODIFIER | c.188+131C>T| |
S191 |
6 | BAA09g04170 | A09 | 2511419 | C | T | intron_variant | MODIFIER | c.189-174C>T| |
S118 |
7 | BAA09g04170 | A09 | 2511565 | G | A | intron_variant | MODIFIER | c.189-28G>A| |
S47 |
8 | BAA09g04170 | A09 | 2512520 | C | T | missense_variant | MODERATE | c.806C>T|p.Ser269Leu |
S216 |
9 | BAA09g04170 | A09 | 2513571 | G | A | downstream_gene_variant | MODIFIER | c.*209G>A| |
S274 |
10 | BAA09g04170 | A09 | 2514145 | G | A | downstream_gene_variant | MODIFIER | c.*783G>A| |
S165 |
11 | BAA09g04170 | A09 | 2514319 | G | A | downstream_gene_variant | MODIFIER | c.*957G>A| |
S201 |
12 | BAA09g04170 | A09 | 2514793 | G | A | downstream_gene_variant | MODIFIER | c.*1431G>A| |
S173 |
13 | BAA09g04170 | A09 | 2515374 | G | A | downstream_gene_variant | MODIFIER | c.*2012G>A| |
S116 |
14 | BAA09g04170 | A09 | 2515833 | G | A | downstream_gene_variant | MODIFIER | c.*2471G>A| |
S218 |
15 | BAA09g04170 | A09 | 2516002 | T | G | downstream_gene_variant | MODIFIER | c.*2640T>G| |
S287 |
16 | BAA09g04170 | A09 | 2516324 | G | A | downstream_gene_variant | MODIFIER | c.*2962G>A| |
S47 |