Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40170 | A02 | 33934040 | G | A | synonymous_variant | LOW | c.3573C>T|p.Ser1191Ser |
S159 S243 |
2 | BAA02g40170 | A02 | 33934437 | C | T | missense_variant | MODERATE | c.3176G>A|p.Arg1059Lys |
S79 S84 |
3 | BAA02g40170 | A02 | 33934553 | G | A | synonymous_variant | LOW | c.3060C>T|p.Phe1020Phe |
S149 |
4 | BAA02g40170 | A02 | 33934935 | C | T | missense_variant | MODERATE | c.2678G>A|p.Arg893Lys |
S51 |
5 | BAA02g40170 | A02 | 33935246 | C | T | splice_region_variant&synonymous_variant | LOW | c.2367G>A|p.Val789Val |
S284 |
6 | BAA02g40170 | A02 | 33937840 | C | T | missense_variant | MODERATE | c.580G>A|p.Val194Met |
S139 |
7 | BAA02g40170 | A02 | 33937880 | C | T | stop_gained | HIGH | c.540G>A|p.Trp180* |
S109 |
8 | BAA02g40170 | A02 | 33938515 | C | T | missense_variant | MODERATE | c.262G>A|p.Ala88Thr |
S157 S163 |
9 | BAA02g40170 | A02 | 33938668 | G | A | intron_variant | MODIFIER | c.238-129C>T| |
S251 |
10 | BAA02g40170 | A02 | 33939236 | G | A | upstream_gene_variant | MODIFIER | c.-104C>T| |
S287 |
11 | BAA02g40170 | A02 | 33941229 | C | T | upstream_gene_variant | MODIFIER | c.-2097G>A| |
S6 |
12 | BAA02g40170 | A02 | 33941377 | G | A | upstream_gene_variant | MODIFIER | c.-2245C>T| |
S297 |
13 | BAA02g40170 | A02 | 33941595 | C | T | upstream_gene_variant | MODIFIER | c.-2463G>A| |
S167 |
14 | BAA02g40170 | A02 | 33942011 | C | T | upstream_gene_variant | MODIFIER | c.-2879G>A| |
S130 |
15 | BAA02g40170 | A02 | 33942242 | C | T | upstream_gene_variant | MODIFIER | c.-3110G>A| |
S139 |
16 | BAA02g40170 | A02 | 33942431 | G | A | upstream_gene_variant | MODIFIER | c.-3299C>T| |
S156 |
17 | BAA02g40170 | A02 | 33943197 | G | A | upstream_gene_variant | MODIFIER | c.-4065C>T| |
S236 |
18 | BAA02g40170 | A02 | 33943231 | C | T | upstream_gene_variant | MODIFIER | c.-4099G>A| |
S202 |
19 | BAA02g40170 | A02 | 33943233 | G | A | upstream_gene_variant | MODIFIER | c.-4101C>T| |
S125 |
20 | BAA02g40170 | A02 | 33943248 | G | A | upstream_gene_variant | MODIFIER | c.-4116C>T| |
S125 |
21 | BAA02g40170 | A02 | 33943464 | C | T | upstream_gene_variant | MODIFIER | c.-4332G>A| |
S74 |
22 | BAA02g40170 | A02 | 33944029 | C | T | upstream_gene_variant | MODIFIER | c.-4897G>A| |
S233 |