Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g11930 | A03 | 4918542 | G | A | synonymous_variant | LOW | c.3507C>T|p.Ser1169Ser |
S296 |
2 | BAA03g11930 | A03 | 4918677 | G | A | synonymous_variant | LOW | c.3372C>T|p.Ile1124Ile |
S98 |
3 | BAA03g11930 | A03 | 4919072 | G | A | missense_variant | MODERATE | c.3152C>T|p.Ser1051Phe |
S109 |
4 | BAA03g11930 | A03 | 4919994 | G | A | intron_variant | MODIFIER | c.2928-168C>T| |
S72 S78 |
5 | BAA03g11930 | A03 | 4920092 | G | A | intron_variant | MODIFIER | c.2928-266C>T| |
S143 |
6 | BAA03g11930 | A03 | 4920427 | G | A | intron_variant | MODIFIER | c.2928-601C>T| |
S94 |
7 | BAA03g11930 | A03 | 4920800 | C | T | intron_variant | MODIFIER | c.2927+694G>A| |
S221 |
8 | BAA03g11930 | A03 | 4921448 | C | T | intron_variant | MODIFIER | c.2927+46G>A| |
S77 S82 |
9 | BAA03g11930 | A03 | 4921638 | T | C | missense_variant | MODERATE | c.2783A>G|p.Tyr928Cys |
S62 |
10 | BAA03g11930 | A03 | 4921749 | C | T | missense_variant | MODERATE | c.2672G>A|p.Gly891Glu |
S278 |
11 | BAA03g11930 | A03 | 4921931 | G | A | intron_variant | MODIFIER | c.2602-112C>T| |
S143 |
12 | BAA03g11930 | A03 | 4923378 | C | T | intron_variant | MODIFIER | c.2601+477G>A| |
S266 |
13 | BAA03g11930 | A03 | 4924599 | G | A | intron_variant | MODIFIER | c.2035+25C>T| |
S69 |
14 | BAA03g11930 | A03 | 4925344 | G | A | missense_variant | MODERATE | c.1597C>T|p.Pro533Ser |
S255 S59 |
15 | BAA03g11930 | A03 | 4927090 | G | A | stop_gained | HIGH | c.607C>T|p.Gln203* |
S43 |
16 | BAA03g11930 | A03 | 4928376 | G | A | upstream_gene_variant | MODIFIER | c.-543C>T| |
S139 |
17 | BAA03g11930 | A03 | 4928683 | G | A | upstream_gene_variant | MODIFIER | c.-850C>T| |
S132 S137 S215 S89 |