Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11730 | A04 | 17660237 | C | T | missense_variant | MODERATE | c.3035G>A|p.Gly1012Glu |
S156 |
2 | BAA04g11730 | A04 | 17660835 | G | A | stop_gained | HIGH | c.2437C>T|p.Arg813* |
S124 |
3 | BAA04g11730 | A04 | 17660984 | G | A | missense_variant | MODERATE | c.2288C>T|p.Pro763Leu |
S223 |
4 | BAA04g11730 | A04 | 17661050 | C | T | missense_variant | MODERATE | c.2222G>A|p.Arg741Lys |
S129 |
5 | BAA04g11730 | A04 | 17661126 | C | T | missense_variant | MODERATE | c.2146G>A|p.Glu716Lys |
S167 |
6 | BAA04g11730 | A04 | 17662065 | G | A | intron_variant | MODIFIER | c.1437+13C>T| |
S282 |
7 | BAA04g11730 | A04 | 17662275 | G | A | missense_variant | MODERATE | c.1327C>T|p.Leu443Phe |
S171 |
8 | BAA04g11730 | A04 | 17662318 | G | A | synonymous_variant | LOW | c.1284C>T|p.Ile428Ile |
S103 S303 |
9 | BAA04g11730 | A04 | 17663738 | G | A | missense_variant | MODERATE | c.419C>T|p.Thr140Ile |
S205 |
10 | BAA04g11730 | A04 | 17663742 | G | A | missense_variant | MODERATE | c.415C>T|p.Pro139Ser |
S177 |
11 | BAA04g11730 | A04 | 17664137 | G | A | intron_variant | MODIFIER | c.265+13C>T| |
S262 |
12 | BAA04g11730 | A04 | 17664283 | G | A | synonymous_variant | LOW | c.132C>T|p.Phe44Phe |
S33 |
13 | BAA04g11730 | A04 | 17664465 | C | T | intron_variant | MODIFIER | c.91-141G>A| |
S237 |
14 | BAA04g11730 | A04 | 17665155 | C | T | upstream_gene_variant | MODIFIER | c.-255G>A| |
S209 |
15 | BAA04g11730 | A04 | 17666863 | G | A | upstream_gene_variant | MODIFIER | c.-1963C>T| |
S1 S90 |
16 | BAA04g11730 | A04 | 17667157 | C | T | upstream_gene_variant | MODIFIER | c.-2257G>A| |
S247 |