Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g12600 | A04 | 18292257 | C | T | missense_variant | MODERATE | c.2287G>A|p.Val763Ile |
S65 |
2 | BAA04g12600 | A04 | 18293064 | C | T | missense_variant | MODERATE | c.1480G>A|p.Gly494Ser |
S279 |
3 | BAA04g12600 | A04 | 18293147 | C | T | missense_variant | MODERATE | c.1397G>A|p.Gly466Glu |
S163 |
4 | BAA04g12600 | A04 | 18293319 | G | A | missense_variant | MODERATE | c.1225C>T|p.Leu409Phe |
S280 |
5 | BAA04g12600 | A04 | 18293444 | G | A | missense_variant | MODERATE | c.1100C>T|p.Ala367Val |
S219 S72 |
6 | BAA04g12600 | A04 | 18293460 | G | A | missense_variant | MODERATE | c.1084C>T|p.Pro362Ser |
S190 |
7 | BAA04g12600 | A04 | 18294030 | C | T | missense_variant | MODERATE | c.514G>A|p.Gly172Ser |
S294 |
8 | BAA04g12600 | A04 | 18296280 | G | A | upstream_gene_variant | MODIFIER | c.-1737C>T| |
S71 |
9 | BAA04g12600 | A04 | 18296691 | G | A | upstream_gene_variant | MODIFIER | c.-2148C>T| |
S211 S227 |
10 | BAA04g12600 | A04 | 18297640 | G | A | upstream_gene_variant | MODIFIER | c.-3097C>T| |
S36 |
11 | BAA04g12600 | A04 | 18298488 | C | T | upstream_gene_variant | MODIFIER | c.-3945G>A| |
S200 |
12 | BAA04g12600 | A04 | 18298490 | C | T | upstream_gene_variant | MODIFIER | c.-3947G>A| |
S232 |