Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19740 | A02 | 10279399 | C | T | intron_variant | MODIFIER | c.3190-3885G>A| |
S267 |
2 | BAA02g19740 | A02 | 10282052 | C | T | intron_variant | MODIFIER | c.3189+2024G>A| |
S275 |
3 | BAA02g19740 | A02 | 10282360 | G | A | intron_variant | MODIFIER | c.3189+1716C>T| |
S265 |
4 | BAA02g19740 | A02 | 10282533 | G | A | intron_variant | MODIFIER | c.3189+1543C>T| |
S210 |
5 | BAA02g19740 | A02 | 10282566 | G | A | intron_variant | MODIFIER | c.3189+1510C>T| |
S245 |
6 | BAA02g19740 | A02 | 10282601 | C | T | intron_variant | MODIFIER | c.3189+1475G>A| |
S166 |
7 | BAA02g19740 | A02 | 10283466 | G | A | intron_variant | MODIFIER | c.3189+610C>T| |
S282 |
8 | BAA02g19740 | A02 | 10284099 | G | A | missense_variant | MODERATE | c.3166C>T|p.Pro1056Ser |
S7 |
9 | BAA02g19740 | A02 | 10284124 | G | A | synonymous_variant | LOW | c.3141C>T|p.His1047His |
S189 |
10 | BAA02g19740 | A02 | 10284226 | C | T | synonymous_variant | LOW | c.3039G>A|p.Ala1013Ala |
S135 |
11 | BAA02g19740 | A02 | 10284430 | G | A | synonymous_variant | LOW | c.2835C>T|p.Leu945Leu |
S193 |
12 | BAA02g19740 | A02 | 10285019 | C | T | missense_variant | MODERATE | c.2246G>A|p.Gly749Glu |
S58 |
13 | BAA02g19740 | A02 | 10285188 | G | A | missense_variant | MODERATE | c.2077C>T|p.His693Tyr |
S303 |
14 | BAA02g19740 | A02 | 10285762 | G | A | missense_variant | MODERATE | c.1577C>T|p.Ser526Leu |
S296 |
15 | BAA02g19740 | A02 | 10285879 | G | A | missense_variant | MODERATE | c.1460C>T|p.Ser487Phe |
S129 |
16 | BAA02g19740 | A02 | 10286587 | C | T | intron_variant | MODIFIER | c.833+14G>A| |
S275 |
17 | BAA02g19740 | A02 | 10286785 | G | A | missense_variant | MODERATE | c.649C>T|p.Pro217Ser |
S282 |
18 | BAA02g19740 | A02 | 10287070 | G | A | missense_variant | MODERATE | c.364C>T|p.Pro122Ser |
S190 |
19 | BAA02g19740 | A02 | 10287211 | G | A | missense_variant | MODERATE | c.223C>T|p.Leu75Phe |
S282 |
20 | BAA02g19740 | A02 | 10287253 | G | A | missense_variant | MODERATE | c.181C>T|p.Pro61Ser |
S240 |
21 | BAA02g19740 | A02 | 10287434 | C | T | intron_variant | MODIFIER | c.103+10G>A| |
S262 |
22 | BAA02g19740 | A02 | 10288423 | C | T | upstream_gene_variant | MODIFIER | c.-877G>A| |
S211 S227 |
23 | BAA02g19740 | A02 | 10288683 | C | T | upstream_gene_variant | MODIFIER | c.-1137G>A| |
S119 |
24 | BAA02g19740 | A02 | 10289113 | C | T | upstream_gene_variant | MODIFIER | c.-1567G>A| |
S183 S198 |
25 | BAA02g19740 | A02 | 10290154 | C | T | upstream_gene_variant | MODIFIER | c.-2608G>A| |
S65 |