Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21780 | A08 | 16444355 | G | A | synonymous_variant | LOW | c.360G>A|p.Glu120Glu |
S273 |
2 | BAA08g21780 | A08 | 16444496 | A | G | synonymous_variant | LOW | c.501A>G|p.Lys167Lys |
S143 |
3 | BAA08g21780 | A08 | 16444502 | T | C | synonymous_variant | LOW | c.507T>C|p.Phe169Phe |
S143 |
4 | BAA08g21780 | A08 | 16444515 | A | G | missense_variant | MODERATE | c.520A>G|p.Lys174Glu |
S143 |
5 | BAA08g21780 | A08 | 16444516 | A | T | missense_variant | MODERATE | c.521A>T|p.Lys174Ile |
S143 |
6 | BAA08g21780 | A08 | 16444526 | A | G | synonymous_variant | LOW | c.531A>G|p.Thr177Thr |
S143 |
7 | BAA08g21780 | A08 | 16444527 | G | A | missense_variant | MODERATE | c.532G>A|p.Glu178Lys |
S143 |
8 | BAA08g21780 | A08 | 16444551 | C | T | missense_variant | MODERATE | c.556C>T|p.Arg186Cys |
S240 |
9 | BAA08g21780 | A08 | 16444773 | G | A | missense_variant | MODERATE | c.646G>A|p.Val216Ile |
S96 |
10 | BAA08g21780 | A08 | 16445253 | C | T | stop_gained | HIGH | c.1126C>T|p.Gln376* |
S90 |
11 | BAA08g21780 | A08 | 16445343 | G | A | missense_variant | MODERATE | c.1216G>A|p.Ala406Thr |
S32 |
12 | BAA08g21780 | A08 | 16446082 | C | T | missense_variant | MODERATE | c.1846C>T|p.Pro616Ser |
S144 |
13 | BAA08g21780 | A08 | 16446132 | G | A | synonymous_variant | LOW | c.1896G>A|p.Arg632Arg |
S164 |
14 | BAA08g21780 | A08 | 16446475 | G | A | missense_variant | MODERATE | c.2137G>A|p.Gly713Arg |
S259 |
15 | BAA08g21780 | A08 | 16446814 | C | T | missense_variant | MODERATE | c.2476C>T|p.Pro826Ser |
S67 |
16 | BAA08g21780 | A08 | 16447233 | C | T | synonymous_variant | LOW | c.2895C>T|p.Tyr965Tyr |
S64 |