Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23770 | A02 | 12948544 | G | A | upstream_gene_variant | MODIFIER | c.-4466G>A| |
S210 S245 |
2 | BAA02g23770 | A02 | 12948735 | C | T | upstream_gene_variant | MODIFIER | c.-4275C>T| |
S40 S49 |
3 | BAA02g23770 | A02 | 12949148 | C | T | upstream_gene_variant | MODIFIER | c.-3862C>T| |
S88 |
4 | BAA02g23770 | A02 | 12949192 | C | T | upstream_gene_variant | MODIFIER | c.-3818C>T| |
S183 S198 |
5 | BAA02g23770 | A02 | 12950798 | C | T | upstream_gene_variant | MODIFIER | c.-2212C>T| |
S283 |
6 | BAA02g23770 | A02 | 12951494 | G | A | upstream_gene_variant | MODIFIER | c.-1516G>A| |
S60 |
7 | BAA02g23770 | A02 | 12952262 | G | A | upstream_gene_variant | MODIFIER | c.-748G>A| |
S55 |
8 | BAA02g23770 | A02 | 12952292 | G | A | upstream_gene_variant | MODIFIER | c.-718G>A| |
S274 |
9 | BAA02g23770 | A02 | 12952575 | T | G | upstream_gene_variant | MODIFIER | c.-435T>G| |
S66 |
10 | BAA02g23770 | A02 | 12953158 | C | T | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S262 |
11 | BAA02g23770 | A02 | 12953378 | C | T | synonymous_variant | LOW | c.369C>T|p.Ala123Ala |
S40 |
12 | BAA02g23770 | A02 | 12954069 | G | A | downstream_gene_variant | MODIFIER | c.*253G>A| |
S199 |
13 | BAA02g23770 | A02 | 12955196 | C | T | downstream_gene_variant | MODIFIER | c.*1380C>T| |
S185 |
14 | BAA02g23770 | A02 | 12955246 | C | T | downstream_gene_variant | MODIFIER | c.*1430C>T| |
S105 S106 |
15 | BAA02g23770 | A02 | 12955440 | C | T | downstream_gene_variant | MODIFIER | c.*1624C>T| |
S200 |
16 | BAA02g23770 | A02 | 12955786 | C | T | downstream_gene_variant | MODIFIER | c.*1970C>T| |
S270 |
17 | BAA02g23770 | A02 | 12956064 | C | T | downstream_gene_variant | MODIFIER | c.*2248C>T| |
S64 |
18 | BAA02g23770 | A02 | 12956432 | C | T | downstream_gene_variant | MODIFIER | c.*2616C>T| |
S119 |