Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11150 | A02 | 5038339 | G | A | downstream_gene_variant | MODIFIER | c.*4057C>T| |
S203 |
2 | BAA02g11150 | A02 | 5038871 | C | T | downstream_gene_variant | MODIFIER | c.*3525G>A| |
S299 |
3 | BAA02g11150 | A02 | 5038882 | C | T | downstream_gene_variant | MODIFIER | c.*3514G>A| |
S262 |
4 | BAA02g11150 | A02 | 5038941 | C | T | downstream_gene_variant | MODIFIER | c.*3455G>A| |
S167 |
5 | BAA02g11150 | A02 | 5040656 | G | A | downstream_gene_variant | MODIFIER | c.*1740C>T| |
S41 |
6 | BAA02g11150 | A02 | 5040875 | C | T | downstream_gene_variant | MODIFIER | c.*1521G>A| |
S13 |
7 | BAA02g11150 | A02 | 5043111 | C | T | missense_variant | MODERATE | c.1937G>A|p.Gly646Glu |
S131 |
8 | BAA02g11150 | A02 | 5043153 | C | T | missense_variant | MODERATE | c.1895G>A|p.Gly632Glu |
S181 |
9 | BAA02g11150 | A02 | 5043280 | C | T | missense_variant | MODERATE | c.1768G>A|p.Asp590Asn |
S230 |
10 | BAA02g11150 | A02 | 5043520 | G | A | missense_variant | MODERATE | c.1528C>T|p.Arg510Cys |
S283 |
11 | BAA02g11150 | A02 | 5044323 | C | T | missense_variant | MODERATE | c.989G>A|p.Arg330His |
S40 S49 |
12 | BAA02g11150 | A02 | 5044505 | G | A | intron_variant | MODIFIER | c.931-124C>T| |
S206 S26 |
13 | BAA02g11150 | A02 | 5046561 | C | T | missense_variant | MODERATE | c.208G>A|p.Asp70Asn |
S152 |
14 | BAA02g11150 | A02 | 5047968 | C | T | upstream_gene_variant | MODIFIER | c.-719G>A| |
S193 |
15 | BAA02g11150 | A02 | 5048407 | C | T | upstream_gene_variant | MODIFIER | c.-1158G>A| |
S37 |
16 | BAA02g11150 | A02 | 5048446 | G | A | upstream_gene_variant | MODIFIER | c.-1197C>T| |
S289 S290 |
17 | BAA02g11150 | A02 | 5049093 | C | T | upstream_gene_variant | MODIFIER | c.-1844G>A| |
S257 |
18 | BAA02g11150 | A02 | 5049162 | G | A | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S192 |
19 | BAA02g11150 | A02 | 5050707 | C | T | upstream_gene_variant | MODIFIER | c.-3458G>A| |
S44 |