Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11950 | A06 | 6036804 | G | A | missense_variant | MODERATE | c.857G>A|p.Arg286Lys |
S41 |
2 | BAA06g11950 | A06 | 6036839 | G | A | missense_variant | MODERATE | c.892G>A|p.Val298Ile |
S122 |
3 | BAA06g11950 | A06 | 6038692 | C | T | synonymous_variant | LOW | c.1572C>T|p.Thr524Thr |
S164 |
4 | BAA06g11950 | A06 | 6038986 | C | T | synonymous_variant | LOW | c.1866C>T|p.Phe622Phe |
S20 |
5 | BAA06g11950 | A06 | 6039032 | G | A | missense_variant | MODERATE | c.1912G>A|p.Gly638Arg |
S161 |
6 | BAA06g11950 | A06 | 6039127 | G | A | synonymous_variant | LOW | c.2007G>A|p.Gly669Gly |
S294 |
7 | BAA06g11950 | A06 | 6041239 | G | A | missense_variant | MODERATE | c.3535G>A|p.Val1179Ile |
S257 |
8 | BAA06g11950 | A06 | 6041446 | G | A | missense_variant | MODERATE | c.3742G>A|p.Ala1248Thr |
S287 |
9 | BAA06g11950 | A06 | 6043932 | G | A | downstream_gene_variant | MODIFIER | c.*1920G>A| |
S136 |
10 | BAA06g11950 | A06 | 6044063 | C | T | downstream_gene_variant | MODIFIER | c.*2051C>T| |
S235 |
11 | BAA06g11950 | A06 | 6046895 | G | A | downstream_gene_variant | MODIFIER | c.*4883G>A| |
S113 |