Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g03120 | A06 | 1804069 | G | A | stop_gained | HIGH | c.5074C>T|p.Gln1692* |
S294 |
2 | BAA06g03120 | A06 | 1805549 | G | A | missense_variant | MODERATE | c.4400C>T|p.Ala1467Val |
S153 |
3 | BAA06g03120 | A06 | 1805928 | G | A | synonymous_variant | LOW | c.4288C>T|p.Leu1430Leu |
S152 |
4 | BAA06g03120 | A06 | 1806509 | C | T | missense_variant | MODERATE | c.4055G>A|p.Arg1352Lys |
S132 S137 |
5 | BAA06g03120 | A06 | 1807223 | C | T | intron_variant | MODIFIER | c.3647+40G>A| |
S231 |
6 | BAA06g03120 | A06 | 1807343 | C | T | synonymous_variant | LOW | c.3567G>A|p.Leu1189Leu |
S202 |
7 | BAA06g03120 | A06 | 1807385 | C | T | synonymous_variant | LOW | c.3525G>A|p.Pro1175Pro |
S130 |
8 | BAA06g03120 | A06 | 1808485 | C | T | missense_variant | MODERATE | c.2731G>A|p.Gly911Arg |
S225 S73 |
9 | BAA06g03120 | A06 | 1809366 | G | A | missense_variant | MODERATE | c.2315C>T|p.Ser772Phe |
S123 |
10 | BAA06g03120 | A06 | 1810291 | G | A | missense_variant | MODERATE | c.1831C>T|p.Pro611Ser |
S81 S85 |
11 | BAA06g03120 | A06 | 1810528 | G | A | intron_variant | MODIFIER | c.1674-80C>T| |
S143 |
12 | BAA06g03120 | A06 | 1811828 | C | T | missense_variant | MODERATE | c.995G>A|p.Arg332Lys |
S230 |
13 | BAA06g03120 | A06 | 1811880 | G | A | synonymous_variant | LOW | c.943C>T|p.Leu315Leu |
S87 |
14 | BAA06g03120 | A06 | 1812553 | C | T | missense_variant | MODERATE | c.403G>A|p.Ala135Thr |
S296 |
15 | BAA06g03120 | A06 | 1812617 | C | T | synonymous_variant | LOW | c.339G>A|p.Lys113Lys |
S207 |
16 | BAA06g03120 | A06 | 1813076 | G | A | upstream_gene_variant | MODIFIER | c.-121C>T| |
S123 |
17 | BAA06g03120 | A06 | 1813926 | C | T | upstream_gene_variant | MODIFIER | c.-971G>A| |
S55 |
18 | BAA06g03120 | A06 | 1814757 | C | T | upstream_gene_variant | MODIFIER | c.-1802G>A| |
S189 |
19 | BAA06g03120 | A06 | 1816929 | C | T | upstream_gene_variant | MODIFIER | c.-3974G>A| |
S103 |
20 | BAA06g03120 | A06 | 1817788 | G | A | upstream_gene_variant | MODIFIER | c.-4833C>T| |
S143 S79 |