Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00320 | A09 | 386151 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1417-1G>A| |
S76 |
2 | BAA09g00320 | A09 | 386360 | C | T | splice_region_variant&synonymous_variant | LOW | c.1416G>A|p.Gln472Gln |
S156 |
3 | BAA09g00320 | A09 | 386688 | C | T | synonymous_variant | LOW | c.1182G>A|p.Leu394Leu |
S203 |
4 | BAA09g00320 | A09 | 387435 | G | A | synonymous_variant | LOW | c.702C>T|p.Leu234Leu |
S69 |
5 | BAA09g00320 | A09 | 387677 | G | A | missense_variant | MODERATE | c.545C>T|p.Thr182Ile |
S23 |
6 | BAA09g00320 | A09 | 388973 | C | T | upstream_gene_variant | MODIFIER | c.-230G>A| |
S273 |
7 | BAA09g00320 | A09 | 389925 | G | A | upstream_gene_variant | MODIFIER | c.-1182C>T| |
S306 S308 |
8 | BAA09g00320 | A09 | 390879 | C | T | upstream_gene_variant | MODIFIER | c.-2136G>A| |
S156 |
9 | BAA09g00320 | A09 | 391536 | G | A | upstream_gene_variant | MODIFIER | c.-2793C>T| |
S164 |
10 | BAA09g00320 | A09 | 392631 | G | A | upstream_gene_variant | MODIFIER | c.-3888C>T| |
S192 |
11 | BAA09g00320 | A09 | 392817 | G | A | upstream_gene_variant | MODIFIER | c.-4074C>T| |
S16 |