Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g19400 | A07 | 25119172 | C | T | missense_variant | MODERATE | c.1715G>A|p.Arg572His |
S149 S170 |
2 | BAA07g19400 | A07 | 25119576 | G | A | synonymous_variant | LOW | c.1311C>T|p.Phe437Phe |
S6 |
3 | BAA07g19400 | A07 | 25119694 | C | T | missense_variant | MODERATE | c.1193G>A|p.Gly398Glu |
S200 |
4 | BAA07g19400 | A07 | 25120125 | C | T | missense_variant | MODERATE | c.836G>A|p.Gly279Glu |
S281 |
5 | BAA07g19400 | A07 | 25120227 | G | A | missense_variant | MODERATE | c.734C>T|p.Pro245Leu |
S184 |
6 | BAA07g19400 | A07 | 25120248 | G | A | missense_variant | MODERATE | c.713C>T|p.Pro238Leu |
S202 |
7 | BAA07g19400 | A07 | 25120325 | C | T | synonymous_variant | LOW | c.636G>A|p.Lys212Lys |
S150 |
8 | BAA07g19400 | A07 | 25120351 | G | A | missense_variant | MODERATE | c.610C>T|p.Pro204Ser |
S7 |
9 | BAA07g19400 | A07 | 25120570 | C | T | missense_variant | MODERATE | c.391G>A|p.Glu131Lys |
S176 |
10 | BAA07g19400 | A07 | 25121379 | C | A | upstream_gene_variant | MODIFIER | c.-159G>T| |
|
11 | BAA07g19400 | A07 | 25122135 | C | T | upstream_gene_variant | MODIFIER | c.-915G>A| |
S230 |
12 | BAA07g19400 | A07 | 25124320 | T | G | upstream_gene_variant | MODIFIER | c.-3100A>C| |
S1 S14 S153 S169 S187 S196 S201 S203 S206 S207 S211 S248 S261 S28 S280 S54 S62 S8 |
13 | BAA07g19400 | A07 | 25125500 | G | A | upstream_gene_variant | MODIFIER | c.-4280C>T| |
S132 S137 S215 S89 |
14 | BAA07g19400 | A07 | 25125703 | C | T | upstream_gene_variant | MODIFIER | c.-4483G>A| |
S212 |