Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g33130 | A07 | 32230940 | C | T | missense_variant | MODERATE | c.860C>T|p.Pro287Leu |
S262 |
2 | BAA07g33130 | A07 | 32230984 | C | T | missense_variant | MODERATE | c.904C>T|p.His302Tyr |
S66 |
3 | BAA07g33130 | A07 | 32230997 | C | T | missense_variant | MODERATE | c.917C>T|p.Pro306Leu |
S127 |
4 | BAA07g33130 | A07 | 32231587 | G | A | missense_variant | MODERATE | c.1346G>A|p.Gly449Asp |
S276 |
5 | BAA07g33130 | A07 | 32231727 | G | A | missense_variant | MODERATE | c.1486G>A|p.Asp496Asn |
S142 |
6 | BAA07g33130 | A07 | 32232073 | G | A | stop_gained | HIGH | c.1832G>A|p.Trp611* |
S70 |
7 | BAA07g33130 | A07 | 32232505 | G | A | stop_gained | HIGH | c.2264G>A|p.Trp755* |
S139 |
8 | BAA07g33130 | A07 | 32232683 | C | T | synonymous_variant | LOW | c.2442C>T|p.Asp814Asp |
S122 |
9 | BAA07g33130 | A07 | 32233711 | C | T | downstream_gene_variant | MODIFIER | c.*713C>T| |
S63 |
10 | BAA07g33130 | A07 | 32234332 | G | A | downstream_gene_variant | MODIFIER | c.*1334G>A| |
S87 |
11 | BAA07g33130 | A07 | 32234669 | C | T | downstream_gene_variant | MODIFIER | c.*1671C>T| |
S293 |
12 | BAA07g33130 | A07 | 32235178 | G | A | downstream_gene_variant | MODIFIER | c.*2180G>A| |
S51 |