Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07230 | A05 | 3539083 | C | T | missense_variant | MODERATE | c.50C>T|p.Thr17Met |
S169 |
2 | BAA05g07230 | A05 | 3539675 | G | A | missense_variant | MODERATE | c.642G>A|p.Met214Ile |
S11 |
3 | BAA05g07230 | A05 | 3540117 | G | A | missense_variant | MODERATE | c.1084G>A|p.Glu362Lys |
S282 |
4 | BAA05g07230 | A05 | 3540242 | G | A | synonymous_variant | LOW | c.1209G>A|p.Gly403Gly |
S56 |
5 | BAA05g07230 | A05 | 3540638 | G | A | synonymous_variant | LOW | c.1605G>A|p.Arg535Arg |
S139 |
6 | BAA05g07230 | A05 | 3541162 | C | T | synonymous_variant | LOW | c.2064C>T|p.Pro688Pro |
S75 S81 |
7 | BAA05g07230 | A05 | 3541434 | C | T | missense_variant | MODERATE | c.2336C>T|p.Ser779Phe |
S169 |
8 | BAA05g07230 | A05 | 3543146 | G | A | missense_variant | MODERATE | c.4048G>A|p.Ala1350Thr |
S219 S72 |
9 | BAA05g07230 | A05 | 3543308 | C | T | stop_gained | HIGH | c.4210C>T|p.Gln1404* |
S157 |
10 | BAA05g07230 | A05 | 3543355 | G | A | stop_gained | HIGH | c.4257G>A|p.Trp1419* |
S16 |
11 | BAA05g07230 | A05 | 3544172 | C | T | missense_variant | MODERATE | c.5074C>T|p.Pro1692Ser |
S35 |
12 | BAA05g07230 | A05 | 3544378 | G | A | synonymous_variant | LOW | c.5280G>A|p.Ala1760Ala |
S233 |
13 | BAA05g07230 | A05 | 3545412 | C | T | missense_variant | MODERATE | c.6314C>T|p.Ser2105Phe |
S103 |
14 | BAA05g07230 | A05 | 3545535 | C | T | missense_variant | MODERATE | c.6437C>T|p.Ser2146Phe |
S266 |
15 | BAA05g07230 | A05 | 3546458 | C | T | downstream_gene_variant | MODIFIER | c.*490C>T| |
S130 |
16 | BAA05g07230 | A05 | 3546479 | G | A | downstream_gene_variant | MODIFIER | c.*511G>A| |
S288 |