Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00570 | A09 | 516999 | G | A | missense_variant | MODERATE | c.1739C>T|p.Thr580Ile |
S276 |
2 | BAA09g00570 | A09 | 517079 | C | T | missense_variant | MODERATE | c.1659G>A|p.Met553Ile |
S270 |
3 | BAA09g00570 | A09 | 517118 | G | A | synonymous_variant | LOW | c.1620C>T|p.Ile540Ile |
S218 |
4 | BAA09g00570 | A09 | 517135 | C | T | missense_variant | MODERATE | c.1603G>A|p.Glu535Lys |
S87 |
5 | BAA09g00570 | A09 | 518110 | C | T | missense_variant | MODERATE | c.865G>A|p.Val289Ile |
S182 |
6 | BAA09g00570 | A09 | 518306 | G | A | missense_variant | MODERATE | c.767C>T|p.Thr256Ile |
S167 |
7 | BAA09g00570 | A09 | 518620 | G | A | missense_variant | MODERATE | c.520C>T|p.Pro174Ser |
S299 |
8 | BAA09g00570 | A09 | 519169 | C | T | missense_variant | MODERATE | c.335G>A|p.Arg112Lys |
S150 |
9 | BAA09g00570 | A09 | 519399 | G | A | synonymous_variant | LOW | c.105C>T|p.Ile35Ile |
S293 |
10 | BAA09g00570 | A09 | 519746 | C | T | upstream_gene_variant | MODIFIER | c.-243G>A| |
S104 S52 |
11 | BAA09g00570 | A09 | 519812 | C | T | upstream_gene_variant | MODIFIER | c.-309G>A| |
S39 |
12 | BAA09g00570 | A09 | 521254 | C | T | upstream_gene_variant | MODIFIER | c.-1751G>A| |
S203 |
13 | BAA09g00570 | A09 | 522165 | C | T | upstream_gene_variant | MODIFIER | c.-2662G>A| |
S111 |
14 | BAA09g00570 | A09 | 524013 | C | T | upstream_gene_variant | MODIFIER | c.-4510G>A| |
S18 |