Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g29860 | A04 | 28690954 | G | A | intron_variant | MODIFIER | c.1033-9G>A| |
S211 S227 |
2 | BAA04g29860 | A04 | 28691696 | G | A | missense_variant | MODERATE | c.1348G>A|p.Val450Ile |
S183 |
3 | BAA04g29860 | A04 | 28691961 | G | A | intron_variant | MODIFIER | c.1431+182G>A| |
S79 S91 |
4 | BAA04g29860 | A04 | 28693344 | C | T | missense_variant | MODERATE | c.2110C>T|p.Arg704Cys |
S95 |
5 | BAA04g29860 | A04 | 28693826 | G | A | missense_variant | MODERATE | c.2348G>A|p.Cys783Tyr |
S46 |
6 | BAA04g29860 | A04 | 28694145 | G | A | splice_region_variant&intron_variant | LOW | c.2504+6G>A| |
S233 |
7 | BAA04g29860 | A04 | 28695108 | C | T | intron_variant | MODIFIER | c.2707+94C>T| |
S68 |
8 | BAA04g29860 | A04 | 28695646 | G | A | missense_variant | MODERATE | c.2989G>A|p.Gly997Arg |
S179 |
9 | BAA04g29860 | A04 | 28696190 | C | T | missense_variant | MODERATE | c.3307C>T|p.Pro1103Ser |
S240 |
10 | BAA04g29860 | A04 | 28698863 | C | T | intron_variant | MODIFIER | c.4705-23C>T| |
S224 |
11 | BAA04g29860 | A04 | 28699915 | G | A | downstream_gene_variant | MODIFIER | c.*853G>A| |
S240 |
12 | BAA04g29860 | A04 | 28700074 | G | A | downstream_gene_variant | MODIFIER | c.*1012G>A| |
S74 |
13 | BAA04g29860 | A04 | 28700547 | C | T | downstream_gene_variant | MODIFIER | c.*1485C>T| |
S42 |
14 | BAA04g29860 | A04 | 28701930 | G | A | downstream_gene_variant | MODIFIER | c.*2868G>A| |
S262 |
15 | BAA04g29860 | A04 | 28702339 | C | T | downstream_gene_variant | MODIFIER | c.*3277C>T| |
S2 |
16 | BAA04g29860 | A04 | 28702754 | C | T | downstream_gene_variant | MODIFIER | c.*3692C>T| |
S107 |
17 | BAA04g29860 | A04 | 28703508 | G | A | downstream_gene_variant | MODIFIER | c.*4446G>A| |
S278 |
18 | BAA04g29860 | A04 | 28703612 | C | T | downstream_gene_variant | MODIFIER | c.*4550C>T| |
S262 |