Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g24980 | A06 | 16915126 | C | T | missense_variant | MODERATE | c.1684C>T|p.Pro562Ser |
S111 |
2 | BAA06g24980 | A06 | 16915206 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1693-1G>A| |
S48 |
3 | BAA06g24980 | A06 | 16915897 | G | A | missense_variant | MODERATE | c.2023G>A|p.Glu675Lys |
S90 |
4 | BAA06g24980 | A06 | 16916084 | C | T | missense_variant | MODERATE | c.2210C>T|p.Thr737Ile |
S256 |
5 | BAA06g24980 | A06 | 16916181 | G | A | synonymous_variant | LOW | c.2307G>A|p.Gln769Gln |
S180 |
6 | BAA06g24980 | A06 | 16916193 | C | T | synonymous_variant | LOW | c.2319C>T|p.Cys773Cys |
S116 |
7 | BAA06g24980 | A06 | 16916647 | C | T | missense_variant | MODERATE | c.2597C>T|p.Thr866Ile |
S68 |
8 | BAA06g24980 | A06 | 16916775 | G | A | missense_variant | MODERATE | c.2725G>A|p.Glu909Lys |
S179 |
9 | BAA06g24980 | A06 | 16917019 | C | T | missense_variant | MODERATE | c.2969C>T|p.Ser990Phe |
S58 |
10 | BAA06g24980 | A06 | 16917053 | G | A | missense_variant | MODERATE | c.3003G>A|p.Met1001Ile |
S257 |