Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18970 | A01 | 9301281 | C | T | upstream_gene_variant | MODIFIER | c.-4175C>T| |
S259 |
2 | BAA01g18970 | A01 | 9306432 | G | A | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S180 |
3 | BAA01g18970 | A01 | 9307260 | C | T | missense_variant | MODERATE | c.1535C>T|p.Ala512Val |
S286 |
4 | BAA01g18970 | A01 | 9307277 | G | A | missense_variant | MODERATE | c.1552G>A|p.Ala518Thr |
S87 |
5 | BAA01g18970 | A01 | 9308815 | G | A | missense_variant | MODERATE | c.2579G>A|p.Arg860Lys |
S13 |
6 | BAA01g18970 | A01 | 9309369 | C | T | missense_variant | MODERATE | c.3133C>T|p.Pro1045Ser |
S179 |
7 | BAA01g18970 | A01 | 9309854 | G | A | synonymous_variant | LOW | c.3618G>A|p.Lys1206Lys |
S225 S73 |
8 | BAA01g18970 | A01 | 9310086 | C | T | synonymous_variant | LOW | c.3850C>T|p.Leu1284Leu |
S81 S85 |
9 | BAA01g18970 | A01 | 9310777 | C | T | missense_variant | MODERATE | c.4541C>T|p.Ala1514Val |
S107 |
10 | BAA01g18970 | A01 | 9310919 | C | T | synonymous_variant | LOW | c.4683C>T|p.Asp1561Asp |
S50 |
11 | BAA01g18970 | A01 | 9311808 | C | T | missense_variant | MODERATE | c.5572C>T|p.Leu1858Phe |
S264 |
12 | BAA01g18970 | A01 | 9312273 | G | A | splice_region_variant&intron_variant | LOW | c.5940+7G>A| |
S143 |
13 | BAA01g18970 | A01 | 9312610 | G | A | missense_variant | MODERATE | c.6002G>A|p.Gly2001Glu |
S232 |
14 | BAA01g18970 | A01 | 9312975 | C | T | missense_variant | MODERATE | c.6275C>T|p.Ser2092Phe |
S270 |