Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19180 | A09 | 11661095 | G | A | upstream_gene_variant | MODIFIER | c.-3309G>A| |
S166 |
2 | BAA09g19180 | A09 | 11662037 | C | T | upstream_gene_variant | MODIFIER | c.-2367C>T| |
S237 |
3 | BAA09g19180 | A09 | 11662107 | G | A | upstream_gene_variant | MODIFIER | c.-2297G>A| |
S262 |
4 | BAA09g19180 | A09 | 11663871 | C | T | upstream_gene_variant | MODIFIER | c.-533C>T| |
S274 S303 |
5 | BAA09g19180 | A09 | 11665487 | C | T | synonymous_variant | LOW | c.867C>T|p.Leu289Leu |
S95 |
6 | BAA09g19180 | A09 | 11665715 | C | T | synonymous_variant | LOW | c.1095C>T|p.Pro365Pro |
S67 |
7 | BAA09g19180 | A09 | 11666187 | C | T | missense_variant | MODERATE | c.1567C>T|p.Leu523Phe |
S13 S278 S279 |
8 | BAA09g19180 | A09 | 11666257 | C | T | missense_variant | MODERATE | c.1637C>T|p.Ser546Leu |
S46 |
9 | BAA09g19180 | A09 | 11666275 | C | T | missense_variant | MODERATE | c.1655C>T|p.Pro552Leu |
S71 |
10 | BAA09g19180 | A09 | 11666376 | C | T | stop_gained | HIGH | c.1756C>T|p.Gln586* |
S11 |
11 | BAA09g19180 | A09 | 11669505 | G | A | downstream_gene_variant | MODIFIER | c.*3115G>A| |
S238 |
12 | BAA09g19180 | A09 | 11670166 | C | T | downstream_gene_variant | MODIFIER | c.*3776C>T| |
S103 |