Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13430 | A02 | 6113729 | C | T | missense_variant | MODERATE | c.3014G>A|p.Gly1005Glu |
S289 S290 |
2 | BAA02g13430 | A02 | 6116033 | C | T | missense_variant | MODERATE | c.2203G>A|p.Glu735Lys |
S135 |
3 | BAA02g13430 | A02 | 6116158 | G | A | missense_variant | MODERATE | c.2078C>T|p.Ala693Val |
S282 |
4 | BAA02g13430 | A02 | 6117701 | C | T | intron_variant | MODIFIER | c.1392-769G>A| |
S289 S290 |
5 | BAA02g13430 | A02 | 6118197 | G | A | intron_variant | MODIFIER | c.1391+842C>T| |
S59 |
6 | BAA02g13430 | A02 | 6119126 | C | T | missense_variant | MODERATE | c.1304G>A|p.Arg435Gln |
S94 |
7 | BAA02g13430 | A02 | 6119141 | A | C | missense_variant | MODERATE | c.1289T>G|p.Met430Arg |
S112 S178 |
8 | BAA02g13430 | A02 | 6119566 | G | A | synonymous_variant | LOW | c.864C>T|p.Ser288Ser |
S271 |
9 | BAA02g13430 | A02 | 6120018 | G | A | stop_gained | HIGH | c.412C>T|p.Gln138* |
S169 |
10 | BAA02g13430 | A02 | 6122002 | C | T | upstream_gene_variant | MODIFIER | c.-1474G>A| |
S201 |
11 | BAA02g13430 | A02 | 6122109 | C | T | upstream_gene_variant | MODIFIER | c.-1581G>A| |
S267 |
12 | BAA02g13430 | A02 | 6122224 | G | A | upstream_gene_variant | MODIFIER | c.-1696C>T| |
S25 |
13 | BAA02g13430 | A02 | 6123134 | C | T | upstream_gene_variant | MODIFIER | c.-2606G>A| |
S292 |
14 | BAA02g13430 | A02 | 6123170 | G | A | upstream_gene_variant | MODIFIER | c.-2642C>T| |
S191 |