Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g64730 | A03 | 38281157 | G | A | missense_variant | MODERATE | c.1391C>T|p.Ala464Val |
S169 |
2 | BAA03g64730 | A03 | 38281306 | G | A | synonymous_variant | LOW | c.1242C>T|p.Ile414Ile |
S95 |
3 | BAA03g64730 | A03 | 38282039 | G | A | missense_variant | MODERATE | c.940C>T|p.Arg314Cys |
S249 |
4 | BAA03g64730 | A03 | 38282163 | G | A | synonymous_variant | LOW | c.816C>T|p.Arg272Arg |
S303 |
5 | BAA03g64730 | A03 | 38282909 | G | A | intron_variant | MODIFIER | c.590+82C>T| |
S28 |
6 | BAA03g64730 | A03 | 38283317 | C | T | synonymous_variant | LOW | c.264G>A|p.Gln88Gln |
S211 S227 |
7 | BAA03g64730 | A03 | 38283445 | C | T | missense_variant | MODERATE | c.136G>A|p.Val46Met |
S298 |
8 | BAA03g64730 | A03 | 38284327 | A | C | upstream_gene_variant | MODIFIER | c.-747T>G| |
S206 S26 |
9 | BAA03g64730 | A03 | 38284551 | C | T | upstream_gene_variant | MODIFIER | c.-971G>A| |
S194 |
10 | BAA03g64730 | A03 | 38284891 | T | A | upstream_gene_variant | MODIFIER | c.-1311A>T| |
S97 |
11 | BAA03g64730 | A03 | 38285270 | G | A | upstream_gene_variant | MODIFIER | c.-1690C>T| |
S261 |
12 | BAA03g64730 | A03 | 38286493 | G | A | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S6 |
13 | BAA03g64730 | A03 | 38287372 | C | T | upstream_gene_variant | MODIFIER | c.-3792G>A| |
S113 |
14 | BAA03g64730 | A03 | 38287912 | C | T | upstream_gene_variant | MODIFIER | c.-4332G>A| |
S15 S3 |
15 | BAA03g64730 | A03 | 38288163 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S190 |