Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22220 | A09 | 13875954 | G | A | missense_variant | MODERATE | c.3214C>T|p.Pro1072Ser |
S209 |
2 | BAA09g22220 | A09 | 13877016 | C | T | missense_variant | MODERATE | c.2152G>A|p.Gly718Arg |
S245 |
3 | BAA09g22220 | A09 | 13877142 | G | A | missense_variant | MODERATE | c.2026C>T|p.Leu676Phe |
S192 |
4 | BAA09g22220 | A09 | 13877627 | C | T | missense_variant | MODERATE | c.1541G>A|p.Cys514Tyr |
S287 |
5 | BAA09g22220 | A09 | 13877783 | G | A | missense_variant | MODERATE | c.1385C>T|p.Ser462Leu |
S166 |
6 | BAA09g22220 | A09 | 13877923 | A | T | missense_variant | MODERATE | c.1245T>A|p.Asp415Glu |
S275 |
7 | BAA09g22220 | A09 | 13878597 | G | A | stop_gained | HIGH | c.571C>T|p.Gln191* |
S70 |
8 | BAA09g22220 | A09 | 13878645 | G | A | synonymous_variant | LOW | c.523C>T|p.Leu175Leu |
S246 |
9 | BAA09g22220 | A09 | 13879860 | C | T | upstream_gene_variant | MODIFIER | c.-693G>A| |
S50 |
10 | BAA09g22220 | A09 | 13879910 | C | T | upstream_gene_variant | MODIFIER | c.-743G>A| |
S237 S250 |
11 | BAA09g22220 | A09 | 13880067 | C | T | upstream_gene_variant | MODIFIER | c.-900G>A| |
S135 |
12 | BAA09g22220 | A09 | 13880671 | C | T | upstream_gene_variant | MODIFIER | c.-1504G>A| |
S111 |
13 | BAA09g22220 | A09 | 13881553 | C | T | upstream_gene_variant | MODIFIER | c.-2386G>A| |
S82 S92 |
14 | BAA09g22220 | A09 | 13881765 | G | A | upstream_gene_variant | MODIFIER | c.-2598C>T| |
S184 |
15 | BAA09g22220 | A09 | 13882336 | G | A | upstream_gene_variant | MODIFIER | c.-3169C>T| |
S134 |
16 | BAA09g22220 | A09 | 13882378 | C | T | upstream_gene_variant | MODIFIER | c.-3211G>A| |
S148 S210 |