Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g36440 | A08 | 22917550 | C | T | upstream_gene_variant | MODIFIER | c.-1266C>T| |
S302 |
2 | BAA08g36440 | A08 | 22918663 | G | A | upstream_gene_variant | MODIFIER | c.-153G>A| |
S276 |
3 | BAA08g36440 | A08 | 22918867 | G | A | missense_variant | MODERATE | c.52G>A|p.Val18Ile |
S136 |
4 | BAA08g36440 | A08 | 22918882 | C | T | missense_variant | MODERATE | c.67C>T|p.His23Tyr |
S76 |
5 | BAA08g36440 | A08 | 22919224 | A | T | synonymous_variant | LOW | c.228A>T|p.Ala76Ala |
S147 S91 |
6 | BAA08g36440 | A08 | 22919228 | G | T | stop_gained | HIGH | c.232G>T|p.Glu78* |
S147 S91 |
7 | BAA08g36440 | A08 | 22919229 | A | T | missense_variant | MODERATE | c.233A>T|p.Glu78Val |
S147 S91 |
8 | BAA08g36440 | A08 | 22919230 | A | T | missense_variant | MODERATE | c.234A>T|p.Glu78Asp |
S147 S91 |
9 | BAA08g36440 | A08 | 22919234 | G | T | missense_variant | MODERATE | c.238G>T|p.Ala80Ser |
S147 S91 |
10 | BAA08g36440 | A08 | 22919245 | G | A | synonymous_variant | LOW | c.249G>A|p.Gly83Gly |
S147 S91 |
11 | BAA08g36440 | A08 | 22919255 | C | G | missense_variant | MODERATE | c.259C>G|p.Leu87Val |
S147 S91 |
12 | BAA08g36440 | A08 | 22919260 | G | C | synonymous_variant | LOW | c.264G>C|p.Ser88Ser |
S147 S91 |
13 | BAA08g36440 | A08 | 22919262 | C | T | missense_variant | MODERATE | c.266C>T|p.Pro89Leu |
S147 S91 |
14 | BAA08g36440 | A08 | 22919264 | G | A | missense_variant | MODERATE | c.268G>A|p.Gly90Ser |
S204 |