Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15050 | A09 | 8606848 | G | A | missense_variant | MODERATE | c.2362C>T|p.Pro788Ser |
S265 |
2 | BAA09g15050 | A09 | 8607002 | G | A | synonymous_variant | LOW | c.2208C>T|p.Leu736Leu |
S144 |
3 | BAA09g15050 | A09 | 8607426 | G | A | missense_variant | MODERATE | c.1850C>T|p.Pro617Leu |
S202 |
4 | BAA09g15050 | A09 | 8607589 | G | A | missense_variant | MODERATE | c.1687C>T|p.Arg563Trp |
S98 |
5 | BAA09g15050 | A09 | 8608156 | G | A | synonymous_variant | LOW | c.1293C>T|p.Tyr431Tyr |
S189 |
6 | BAA09g15050 | A09 | 8608334 | G | A | missense_variant | MODERATE | c.1115C>T|p.Pro372Leu |
S240 |
7 | BAA09g15050 | A09 | 8609236 | G | A | missense_variant | MODERATE | c.653C>T|p.Ser218Phe |
S61 |
8 | BAA09g15050 | A09 | 8609481 | G | A | synonymous_variant | LOW | c.408C>T|p.Tyr136Tyr |
S288 |
9 | BAA09g15050 | A09 | 8610961 | G | A | upstream_gene_variant | MODIFIER | c.-884C>T| |
S274 |
10 | BAA09g15050 | A09 | 8611034 | C | T | upstream_gene_variant | MODIFIER | c.-957G>A| |
S148 S210 |
11 | BAA09g15050 | A09 | 8611276 | C | T | upstream_gene_variant | MODIFIER | c.-1199G>A| |
S275 |
12 | BAA09g15050 | A09 | 8611472 | G | A | upstream_gene_variant | MODIFIER | c.-1395C>T| |
S57 |
13 | BAA09g15050 | A09 | 8611848 | C | T | upstream_gene_variant | MODIFIER | c.-1771G>A| |
S8 |
14 | BAA09g15050 | A09 | 8612518 | C | T | upstream_gene_variant | MODIFIER | c.-2441G>A| |
S288 |
15 | BAA09g15050 | A09 | 8612738 | C | T | upstream_gene_variant | MODIFIER | c.-2661G>A| |
S30 S31 |
16 | BAA09g15050 | A09 | 8612927 | C | T | upstream_gene_variant | MODIFIER | c.-2850G>A| |
S6 |
17 | BAA09g15050 | A09 | 8613209 | G | A | upstream_gene_variant | MODIFIER | c.-3132C>T| |
S69 |
18 | BAA09g15050 | A09 | 8614609 | G | A | upstream_gene_variant | MODIFIER | c.-4532C>T| |
S264 |