Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g31950 | A09 | 40499485 | C | T | downstream_gene_variant | MODIFIER | c.*876G>A| |
S245 |
2 | BAA09g31950 | A09 | 40500920 | G | A | intron_variant | MODIFIER | c.856-524C>T| |
S103 |
3 | BAA09g31950 | A09 | 40501107 | C | T | intron_variant | MODIFIER | c.855+581G>A| |
S61 |
4 | BAA09g31950 | A09 | 40501194 | G | A | intron_variant | MODIFIER | c.855+494C>T| |
S155 S211 |
5 | BAA09g31950 | A09 | 40501299 | C | T | intron_variant | MODIFIER | c.855+389G>A| |
S205 |
6 | BAA09g31950 | A09 | 40501814 | G | A | synonymous_variant | LOW | c.729C>T|p.Phe243Phe |
S231 |
7 | BAA09g31950 | A09 | 40501845 | G | A | missense_variant | MODERATE | c.698C>T|p.Ser233Leu |
S226 |
8 | BAA09g31950 | A09 | 40502164 | G | A | splice_region_variant&intron_variant | LOW | c.385-6C>T| |
S105 S106 |
9 | BAA09g31950 | A09 | 40502336 | G | A | stop_gained | HIGH | c.274C>T|p.Gln92* |
S216 |
10 | BAA09g31950 | A09 | 40502604 | C | T | missense_variant | MODERATE | c.96G>A|p.Met32Ile |
S56 |
11 | BAA09g31950 | A09 | 40502722 | C | T | intron_variant | MODIFIER | c.51-73G>A| |
S242 |
12 | BAA09g31950 | A09 | 40507246 | G | A | upstream_gene_variant | MODIFIER | c.-4274C>T| |
S279 |
13 | BAA09g31950 | A09 | 40507762 | G | A | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S174 S216 S27 S39 |