Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11670 | A02 | 5272210 | C | T | missense_variant | MODERATE | c.2251G>A|p.Asp751Asn |
S275 |
2 | BAA02g11670 | A02 | 5272914 | G | A | missense_variant | MODERATE | c.1835C>T|p.Ser612Phe |
S229 |
3 | BAA02g11670 | A02 | 5273244 | G | A | missense_variant | MODERATE | c.1585C>T|p.Leu529Phe |
S190 |
4 | BAA02g11670 | A02 | 5274623 | C | T | stop_gained | HIGH | c.669G>A|p.Trp223* |
S127 |
5 | BAA02g11670 | A02 | 5274662 | C | T | synonymous_variant | LOW | c.630G>A|p.Pro210Pro |
S250 |
6 | BAA02g11670 | A02 | 5275352 | G | A | synonymous_variant | LOW | c.286C>T|p.Leu96Leu |
S287 |
7 | BAA02g11670 | A02 | 5275502 | C | T | missense_variant | MODERATE | c.136G>A|p.Glu46Lys |
S157 S163 |
8 | BAA02g11670 | A02 | 5275513 | G | A | missense_variant | MODERATE | c.125C>T|p.Ser42Phe |
S165 |
9 | BAA02g11670 | A02 | 5276635 | C | T | upstream_gene_variant | MODIFIER | c.-880G>A| |
S234 |
10 | BAA02g11670 | A02 | 5279348 | C | T | upstream_gene_variant | MODIFIER | c.-3593G>A| |
S196 |
11 | BAA02g11670 | A02 | 5279807 | G | A | upstream_gene_variant | MODIFIER | c.-4052C>T| |
S232 |
12 | BAA02g11670 | A02 | 5280147 | C | T | upstream_gene_variant | MODIFIER | c.-4392G>A| |
S268 |