Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26500 | A05 | 31115762 | G | A | downstream_gene_variant | MODIFIER | c.*2968C>T| |
S231 |
2 | BAA05g26500 | A05 | 31115786 | G | A | downstream_gene_variant | MODIFIER | c.*2944C>T| |
S62 |
3 | BAA05g26500 | A05 | 31116298 | C | T | downstream_gene_variant | MODIFIER | c.*2432G>A| |
S99 |
4 | BAA05g26500 | A05 | 31119127 | G | A | missense_variant | MODERATE | c.1226C>T|p.Ser409Phe |
S66 |
5 | BAA05g26500 | A05 | 31119187 | G | A | missense_variant | MODERATE | c.1166C>T|p.Pro389Leu |
S200 |
6 | BAA05g26500 | A05 | 31119247 | G | A | missense_variant | MODERATE | c.1106C>T|p.Ser369Leu |
S103 |
7 | BAA05g26500 | A05 | 31120412 | G | A | intron_variant | MODIFIER | c.625+91C>T| |
S44 |
8 | BAA05g26500 | A05 | 31120817 | C | T | missense_variant | MODERATE | c.452G>A|p.Gly151Asp |
S175 |
9 | BAA05g26500 | A05 | 31120971 | C | T | missense_variant | MODERATE | c.298G>A|p.Val100Ile |
S13 |
10 | BAA05g26500 | A05 | 31121778 | G | A | upstream_gene_variant | MODIFIER | c.-433C>T| |
S260 |
11 | BAA05g26500 | A05 | 31122576 | G | A | upstream_gene_variant | MODIFIER | c.-1231C>T| |
S75 S81 |
12 | BAA05g26500 | A05 | 31123238 | G | A | upstream_gene_variant | MODIFIER | c.-1893C>T| |
S283 |
13 | BAA05g26500 | A05 | 31123426 | C | T | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S13 S168 S219 S64 |
14 | BAA05g26500 | A05 | 31123428 | G | A | upstream_gene_variant | MODIFIER | c.-2083C>T| |
S278 |
15 | BAA05g26500 | A05 | 31123613 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S45 |
16 | BAA05g26500 | A05 | 31124603 | G | A | upstream_gene_variant | MODIFIER | c.-3258C>T| |
S40 S49 |
17 | BAA05g26500 | A05 | 31124626 | C | T | upstream_gene_variant | MODIFIER | c.-3281G>A| |
S273 |