Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g00030 | A03 | 17367 | G | A | missense_variant | MODERATE | c.569G>A|p.Arg190Lys |
S52 |
2 | BAA03g00030 | A03 | 17416 | C | T | synonymous_variant | LOW | c.618C>T|p.Leu206Leu |
S283 |
3 | BAA03g00030 | A03 | 17430 | G | A | missense_variant | MODERATE | c.632G>A|p.Arg211Lys |
S250 |
4 | BAA03g00030 | A03 | 17444 | G | A | missense_variant | MODERATE | c.646G>A|p.Glu216Lys |
S157 |
5 | BAA03g00030 | A03 | 18133 | T | C | synonymous_variant | LOW | c.1335T>C|p.Arg445Arg |
S297 |
6 | BAA03g00030 | A03 | 18382 | G | A | synonymous_variant | LOW | c.1584G>A|p.Arg528Arg |
S286 |
7 | BAA03g00030 | A03 | 18773 | G | A | missense_variant | MODERATE | c.1975G>A|p.Glu659Lys |
S183 S198 |
8 | BAA03g00030 | A03 | 18822 | G | A | missense_variant | MODERATE | c.2024G>A|p.Cys675Tyr |
S276 |
9 | BAA03g00030 | A03 | 18918 | G | A | missense_variant | MODERATE | c.2120G>A|p.Gly707Asp |
S89 |
10 | BAA03g00030 | A03 | 18961 | G | A | synonymous_variant | LOW | c.2163G>A|p.Arg721Arg |
S138 |
11 | BAA03g00030 | A03 | 19259 | G | A | missense_variant | MODERATE | c.2461G>A|p.Glu821Lys |
S150 |
12 | BAA03g00030 | A03 | 19380 | C | T | missense_variant | MODERATE | c.2582C>T|p.Ser861Phe |
S12 S236 |
13 | BAA03g00030 | A03 | 19382 | G | A | missense_variant | MODERATE | c.2584G>A|p.Ala862Thr |
S245 |
14 | BAA03g00030 | A03 | 19957 | C | T | synonymous_variant | LOW | c.3159C>T|p.Leu1053Leu |
S174 S27 |
15 | BAA03g00030 | A03 | 20051 | C | T | missense_variant | MODERATE | c.3253C>T|p.Leu1085Phe |
S45 |
16 | BAA03g00030 | A03 | 20156 | C | T | missense_variant | MODERATE | c.3358C>T|p.Leu1120Phe |
S73 S91 |
17 | BAA03g00030 | A03 | 20511 | C | T | missense_variant | MODERATE | c.3713C>T|p.Ala1238Val |
S174 S27 |