Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g33870 | A10 | 23984236 | C | T | missense_variant | MODERATE | c.3106G>A|p.Ala1036Thr |
S221 |
2 | BAA10g33870 | A10 | 23984769 | G | A | missense_variant | MODERATE | c.2573C>T|p.Ser858Phe |
S70 |
3 | BAA10g33870 | A10 | 23984780 | C | T | synonymous_variant | LOW | c.2562G>A|p.Glu854Glu |
S25 |
4 | BAA10g33870 | A10 | 23985638 | C | T | synonymous_variant | LOW | c.1704G>A|p.Lys568Lys |
S292 |
5 | BAA10g33870 | A10 | 23986914 | C | T | missense_variant | MODERATE | c.580G>A|p.Gly194Arg |
S44 |
6 | BAA10g33870 | A10 | 23989084 | C | T | upstream_gene_variant | MODIFIER | c.-1295G>A| |
S221 |
7 | BAA10g33870 | A10 | 23989130 | C | T | upstream_gene_variant | MODIFIER | c.-1341G>A| |
S186 S296 |
8 | BAA10g33870 | A10 | 23992144 | C | T | upstream_gene_variant | MODIFIER | c.-4355G>A| |
S148 S30 S31 |