Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16130 | A05 | 8873813 | C | T | upstream_gene_variant | MODIFIER | c.-4878C>T| |
S137 S215 |
2 | BAA05g16130 | A05 | 8873871 | G | A | upstream_gene_variant | MODIFIER | c.-4820G>A| |
S301 S304 |
3 | BAA05g16130 | A05 | 8878698 | C | T | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S162 |
4 | BAA05g16130 | A05 | 8878824 | G | A | missense_variant | MODERATE | c.134G>A|p.Gly45Asp |
S75 S81 |
5 | BAA05g16130 | A05 | 8879038 | C | T | missense_variant | MODERATE | c.269C>T|p.Pro90Leu |
S157 |
6 | BAA05g16130 | A05 | 8879322 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.450-1G>A| |
S46 |
7 | BAA05g16130 | A05 | 8881574 | C | T | missense_variant | MODERATE | c.1727C>T|p.Ser576Leu |
S89 |
8 | BAA05g16130 | A05 | 8881650 | G | A | synonymous_variant | LOW | c.1803G>A|p.Ser601Ser |
S149 |
9 | BAA05g16130 | A05 | 8882797 | G | A | downstream_gene_variant | MODIFIER | c.*290G>A| |
S79 S91 |
10 | BAA05g16130 | A05 | 8883010 | G | A | downstream_gene_variant | MODIFIER | c.*503G>A| |
S294 |
11 | BAA05g16130 | A05 | 8883490 | G | A | downstream_gene_variant | MODIFIER | c.*983G>A| |
S246 |
12 | BAA05g16130 | A05 | 8883504 | C | T | downstream_gene_variant | MODIFIER | c.*997C>T| |
S211 S227 |
13 | BAA05g16130 | A05 | 8884740 | G | A | downstream_gene_variant | MODIFIER | c.*2233G>A| |
S124 |
14 | BAA05g16130 | A05 | 8884841 | C | T | downstream_gene_variant | MODIFIER | c.*2334C>T| |
S211 S227 |