Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19600 | A05 | 11615101 | G | A | synonymous_variant | LOW | c.945G>A|p.Lys315Lys |
S80 |
2 | BAA05g19600 | A05 | 11615124 | G | T | missense_variant | MODERATE | c.968G>T|p.Gly323Val |
S15 |
3 | BAA05g19600 | A05 | 11615384 | C | T | missense_variant | MODERATE | c.1132C>T|p.Pro378Ser |
S228 |
4 | BAA05g19600 | A05 | 11616603 | C | T | intron_variant | MODIFIER | c.1387-37C>T| |
S233 |
5 | BAA05g19600 | A05 | 11616931 | C | T | intron_variant | MODIFIER | c.1560+37C>T| |
S181 |
6 | BAA05g19600 | A05 | 11617131 | G | A | intron_variant | MODIFIER | c.1561-196G>A| |
S46 |
7 | BAA05g19600 | A05 | 11617686 | G | A | intron_variant | MODIFIER | c.1773-20G>A| |
S112 |
8 | BAA05g19600 | A05 | 11618518 | G | A | missense_variant | MODERATE | c.1999G>A|p.Ala667Thr |
S240 |
9 | BAA05g19600 | A05 | 11620451 | C | T | downstream_gene_variant | MODIFIER | c.*1120C>T| |
S36 |
10 | BAA05g19600 | A05 | 11620472 | C | T | downstream_gene_variant | MODIFIER | c.*1141C>T| |
S228 |
11 | BAA05g19600 | A05 | 11622889 | C | T | downstream_gene_variant | MODIFIER | c.*3558C>T| |
S180 |
12 | BAA05g19600 | A05 | 11623280 | C | T | downstream_gene_variant | MODIFIER | c.*3949C>T| |
S247 |
13 | BAA05g19600 | A05 | 11623318 | G | A | downstream_gene_variant | MODIFIER | c.*3987G>A| |
S283 |