Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g01040 | A03 | 405424 | G | A | upstream_gene_variant | MODIFIER | c.-1458G>A| |
S47 |
2 | BAA03g01040 | A03 | 406359 | C | T | upstream_gene_variant | MODIFIER | c.-523C>T| |
S164 |
3 | BAA03g01040 | A03 | 406431 | C | T | upstream_gene_variant | MODIFIER | c.-451C>T| |
S184 |
4 | BAA03g01040 | A03 | 406731 | C | T | upstream_gene_variant | MODIFIER | c.-151C>T| |
S2 |
5 | BAA03g01040 | A03 | 407084 | C | T | missense_variant | MODERATE | c.203C>T|p.Ser68Phe |
S15 S3 |
6 | BAA03g01040 | A03 | 407437 | G | A | missense_variant | MODERATE | c.556G>A|p.Ala186Thr |
S128 S265 |
7 | BAA03g01040 | A03 | 407548 | G | A | missense_variant | MODERATE | c.667G>A|p.Ala223Thr |
S123 |
8 | BAA03g01040 | A03 | 408918 | C | T | missense_variant | MODERATE | c.1424C>T|p.Ala475Val |
S215 |
9 | BAA03g01040 | A03 | 409221 | G | A | missense_variant | MODERATE | c.1636G>A|p.Ala546Thr |
S77 S82 |
10 | BAA03g01040 | A03 | 409403 | C | T | synonymous_variant | LOW | c.1818C>T|p.Phe606Phe |
S173 |
11 | BAA03g01040 | A03 | 409535 | C | T | synonymous_variant | LOW | c.1950C>T|p.Phe650Phe |
S207 |
12 | BAA03g01040 | A03 | 409974 | C | T | missense_variant | MODERATE | c.2389C>T|p.Leu797Phe |
S200 |
13 | BAA03g01040 | A03 | 409978 | G | A | missense_variant | MODERATE | c.2393G>A|p.Cys798Tyr |
S206 |
14 | BAA03g01040 | A03 | 410992 | G | A | synonymous_variant | LOW | c.3060G>A|p.Leu1020Leu |
S10 |
15 | BAA03g01040 | A03 | 411224 | C | T | missense_variant | MODERATE | c.3292C>T|p.His1098Tyr |
S221 |
16 | BAA03g01040 | A03 | 411438 | C | T | missense_variant | MODERATE | c.3506C>T|p.Ala1169Val |
S117 |
17 | BAA03g01040 | A03 | 411660 | C | T | missense_variant | MODERATE | c.3728C>T|p.Ser1243Phe |
S122 |
18 | BAA03g01040 | A03 | 411847 | C | T | synonymous_variant | LOW | c.3829C>T|p.Leu1277Leu |
S245 |