Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18960 | A05 | 11032409 | C | T | downstream_gene_variant | MODIFIER | c.*3356G>A| |
S58 |
2 | BAA05g18960 | A05 | 11034578 | C | T | downstream_gene_variant | MODIFIER | c.*1187G>A| |
S105 S106 |
3 | BAA05g18960 | A05 | 11035080 | G | A | downstream_gene_variant | MODIFIER | c.*685C>T| |
S292 |
4 | BAA05g18960 | A05 | 11035244 | C | T | downstream_gene_variant | MODIFIER | c.*521G>A| |
S28 |
5 | BAA05g18960 | A05 | 11036804 | G | A | intron_variant | MODIFIER | c.915-64C>T| |
S79 S84 |
6 | BAA05g18960 | A05 | 11038233 | G | A | missense_variant | MODERATE | c.238C>T|p.His80Tyr |
S206 S26 |
7 | BAA05g18960 | A05 | 11038250 | C | T | missense_variant | MODERATE | c.221G>A|p.Gly74Glu |
S42 |
8 | BAA05g18960 | A05 | 11039340 | G | A | upstream_gene_variant | MODIFIER | c.-755C>T| |
S32 |
9 | BAA05g18960 | A05 | 11039912 | G | A | upstream_gene_variant | MODIFIER | c.-1327C>T| |
S134 |
10 | BAA05g18960 | A05 | 11040389 | C | T | upstream_gene_variant | MODIFIER | c.-1804G>A| |
S247 |
11 | BAA05g18960 | A05 | 11040743 | C | T | upstream_gene_variant | MODIFIER | c.-2158G>A| |
S140 |
12 | BAA05g18960 | A05 | 11041076 | G | A | upstream_gene_variant | MODIFIER | c.-2491C>T| |
S178 |
13 | BAA05g18960 | A05 | 11041193 | G | A | upstream_gene_variant | MODIFIER | c.-2608C>T| |
S125 |
14 | BAA05g18960 | A05 | 11041544 | C | T | upstream_gene_variant | MODIFIER | c.-2959G>A| |
S84 S93 |
15 | BAA05g18960 | A05 | 11041772 | C | T | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S269 |