Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06170 | A01 | 2764128 | C | T | missense_variant | MODERATE | c.1756G>A|p.Glu586Lys |
S64 |
2 | BAA01g06170 | A01 | 2764515 | G | A | missense_variant | MODERATE | c.1369C>T|p.Pro457Ser |
S175 |
3 | BAA01g06170 | A01 | 2764727 | G | A | missense_variant | MODERATE | c.1157C>T|p.Thr386Ile |
S193 |
4 | BAA01g06170 | A01 | 2764802 | G | A | missense_variant | MODERATE | c.1082C>T|p.Pro361Leu |
S281 |
5 | BAA01g06170 | A01 | 2765071 | G | A | synonymous_variant | LOW | c.813C>T|p.Cys271Cys |
S12 |
6 | BAA01g06170 | A01 | 2765460 | C | T | missense_variant | MODERATE | c.424G>A|p.Ala142Thr |
S203 |
7 | BAA01g06170 | A01 | 2765506 | C | T | synonymous_variant | LOW | c.378G>A|p.Glu126Glu |
S167 |
8 | BAA01g06170 | A01 | 2765557 | G | A | synonymous_variant | LOW | c.327C>T|p.Tyr109Tyr |
S262 |
9 | BAA01g06170 | A01 | 2765707 | G | A | synonymous_variant | LOW | c.177C>T|p.Ser59Ser |
S206 |
10 | BAA01g06170 | A01 | 2765937 | G | C | upstream_gene_variant | MODIFIER | c.-54C>G| |
S108 S11 S126 S132 S148 S156 S160 S244 S277 S3 S305 S41 S50 S51 S59 S69 S81 |
11 | BAA01g06170 | A01 | 2766301 | G | A | upstream_gene_variant | MODIFIER | c.-418C>T| |
S115 |
12 | BAA01g06170 | A01 | 2766702 | G | A | upstream_gene_variant | MODIFIER | c.-819C>T| |
S272 |
13 | BAA01g06170 | A01 | 2767699 | C | T | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S76 |
14 | BAA01g06170 | A01 | 2768311 | C | T | upstream_gene_variant | MODIFIER | c.-2428G>A| |
S77 S82 |
15 | BAA01g06170 | A01 | 2769285 | G | A | upstream_gene_variant | MODIFIER | c.-3402C>T| |
S34 |
16 | BAA01g06170 | A01 | 2769771 | G | A | upstream_gene_variant | MODIFIER | c.-3888C>T| |
S134 S193 |
17 | BAA01g06170 | A01 | 2770313 | C | T | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S211 S227 |
18 | BAA01g06170 | A01 | 2770549 | G | A | upstream_gene_variant | MODIFIER | c.-4666C>T| |
S191 |