Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51910 | A09 | 53984643 | C | T | upstream_gene_variant | MODIFIER | c.-1481C>T| |
S303 |
2 | BAA09g51910 | A09 | 53984898 | G | A | upstream_gene_variant | MODIFIER | c.-1226G>A| |
S241 |
3 | BAA09g51910 | A09 | 53986149 | C | T | missense_variant | MODERATE | c.26C>T|p.Ser9Phe |
S118 |
4 | BAA09g51910 | A09 | 53986228 | C | T | synonymous_variant | LOW | c.105C>T|p.Phe35Phe |
S278 |
5 | BAA09g51910 | A09 | 53986300 | C | T | synonymous_variant | LOW | c.177C>T|p.Thr59Thr |
S296 |
6 | BAA09g51910 | A09 | 53987283 | C | T | missense_variant | MODERATE | c.724C>T|p.Pro242Ser |
S104 S52 |
7 | BAA09g51910 | A09 | 53987541 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.895-1G>A| |
S200 |
8 | BAA09g51910 | A09 | 53987573 | C | T | missense_variant | MODERATE | c.926C>T|p.Thr309Ile |
S44 |
9 | BAA09g51910 | A09 | 53987715 | C | T | splice_region_variant&intron_variant | LOW | c.996-8C>T| |
S153 S157 S166 S236 S257 S262 |
10 | BAA09g51910 | A09 | 53988596 | C | T | missense_variant | MODERATE | c.1469C>T|p.Pro490Leu |
S134 |
11 | BAA09g51910 | A09 | 53988718 | G | A | missense_variant | MODERATE | c.1591G>A|p.Val531Met |
S107 |