Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38100 | A09 | 46128320 | C | T | missense_variant | MODERATE | c.2990G>A|p.Arg997Lys |
S180 |
2 | BAA09g38100 | A09 | 46129072 | G | A | missense_variant | MODERATE | c.2509C>T|p.Pro837Ser |
S132 S137 |
3 | BAA09g38100 | A09 | 46129180 | C | T | missense_variant | MODERATE | c.2401G>A|p.Gly801Arg |
S61 |
4 | BAA09g38100 | A09 | 46131274 | G | A | synonymous_variant | LOW | c.753C>T|p.Phe251Phe |
S71 |
5 | BAA09g38100 | A09 | 46131341 | G | A | missense_variant | MODERATE | c.686C>T|p.Ser229Leu |
S107 |
6 | BAA09g38100 | A09 | 46131644 | G | A | missense_variant | MODERATE | c.383C>T|p.Ala128Val |
S112 |
7 | BAA09g38100 | A09 | 46132583 | G | A | missense_variant | MODERATE | c.128C>T|p.Pro43Leu |
S113 |
8 | BAA09g38100 | A09 | 46132964 | G | A | upstream_gene_variant | MODIFIER | c.-254C>T| |
S134 |
9 | BAA09g38100 | A09 | 46133703 | G | A | upstream_gene_variant | MODIFIER | c.-993C>T| |
S185 |
10 | BAA09g38100 | A09 | 46135411 | G | A | upstream_gene_variant | MODIFIER | c.-2701C>T| |
S151 S263 |
11 | BAA09g38100 | A09 | 46136617 | C | T | upstream_gene_variant | MODIFIER | c.-3907G>A| |
S155 S211 |
12 | BAA09g38100 | A09 | 46137227 | G | A | upstream_gene_variant | MODIFIER | c.-4517C>T| |
S42 |