Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g24960 | A05 | 29887884 | G | A | synonymous_variant | LOW | c.1098C>T|p.His366His |
S174 S241 S27 S39 |
2 | BAA05g24960 | A05 | 29887898 | G | A | missense_variant | MODERATE | c.1084C>T|p.His362Tyr |
S308 |
3 | BAA05g24960 | A05 | 29889281 | C | T | intron_variant | MODIFIER | c.866+306G>A| |
S262 |
4 | BAA05g24960 | A05 | 29889756 | C | T | missense_variant | MODERATE | c.697G>A|p.Ala233Thr |
S226 |
5 | BAA05g24960 | A05 | 29889820 | C | T | synonymous_variant | LOW | c.633G>A|p.Ala211Ala |
S202 |
6 | BAA05g24960 | A05 | 29889999 | G | A | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S133 |
7 | BAA05g24960 | A05 | 29890056 | C | T | missense_variant | MODERATE | c.397G>A|p.Val133Ile |
S17 |
8 | BAA05g24960 | A05 | 29890170 | G | A | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S13 |
9 | BAA05g24960 | A05 | 29890792 | C | T | upstream_gene_variant | MODIFIER | c.-340G>A| |
S172 |
10 | BAA05g24960 | A05 | 29891963 | C | T | upstream_gene_variant | MODIFIER | c.-1511G>A| |
S16 |
11 | BAA05g24960 | A05 | 29892172 | C | T | upstream_gene_variant | MODIFIER | c.-1720G>A| |
S27 |
12 | BAA05g24960 | A05 | 29892260 | G | A | upstream_gene_variant | MODIFIER | c.-1808C>T| |
S132 S137 S89 |
13 | BAA05g24960 | A05 | 29892713 | G | A | upstream_gene_variant | MODIFIER | c.-2261C>T| |
S16 |
14 | BAA05g24960 | A05 | 29893305 | G | A | upstream_gene_variant | MODIFIER | c.-2853C>T| |
S265 |
15 | BAA05g24960 | A05 | 29893526 | C | T | upstream_gene_variant | MODIFIER | c.-3074G>A| |
S281 |
16 | BAA05g24960 | A05 | 29893668 | C | T | upstream_gene_variant | MODIFIER | c.-3216G>A| |
S47 |
17 | BAA05g24960 | A05 | 29894938 | G | A | upstream_gene_variant | MODIFIER | c.-4486C>T| |
S134 |