Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00060 | A09 | 210584 | G | A | synonymous_variant | LOW | c.2895C>T|p.Cys965Cys |
S2 |
2 | BAA09g00060 | A09 | 211346 | C | T | missense_variant | MODERATE | c.2468G>A|p.Gly823Glu |
S13 |
3 | BAA09g00060 | A09 | 211419 | G | A | missense_variant | MODERATE | c.2395C>T|p.Leu799Phe |
S271 |
4 | BAA09g00060 | A09 | 211610 | G | A | synonymous_variant | LOW | c.2280C>T|p.Leu760Leu |
S19 |
5 | BAA09g00060 | A09 | 212211 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1911-1G>A| |
S140 |
6 | BAA09g00060 | A09 | 214437 | G | A | synonymous_variant | LOW | c.654C>T|p.Ala218Ala |
S294 |
7 | BAA09g00060 | A09 | 214553 | C | T | missense_variant | MODERATE | c.538G>A|p.Ala180Thr |
S71 |
8 | BAA09g00060 | A09 | 215442 | G | A | synonymous_variant | LOW | c.42C>T|p.Val14Val |
S25 |
9 | BAA09g00060 | A09 | 216771 | C | T | upstream_gene_variant | MODIFIER | c.-1288G>A| |
S11 |
10 | BAA09g00060 | A09 | 216930 | G | A | upstream_gene_variant | MODIFIER | c.-1447C>T| |
S302 |
11 | BAA09g00060 | A09 | 219871 | G | A | upstream_gene_variant | MODIFIER | c.-4388C>T| |
S69 |
12 | BAA09g00060 | A09 | 220026 | C | T | upstream_gene_variant | MODIFIER | c.-4543G>A| |
S202 |