Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g22190 | A05 | 26397764 | C | T | stop_gained | HIGH | c.2613G>A|p.Trp871* |
S94 |
2 | BAA05g22190 | A05 | 26398531 | G | A | missense_variant | MODERATE | c.2069C>T|p.Ser690Phe |
S282 |
3 | BAA05g22190 | A05 | 26398561 | G | A | missense_variant | MODERATE | c.2039C>T|p.Thr680Ile |
S188 |
4 | BAA05g22190 | A05 | 26398747 | C | T | missense_variant | MODERATE | c.1853G>A|p.Ser618Asn |
S192 |
5 | BAA05g22190 | A05 | 26399158 | C | T | missense_variant | MODERATE | c.1567G>A|p.Ala523Thr |
S139 |
6 | BAA05g22190 | A05 | 26399182 | C | T | missense_variant | MODERATE | c.1543G>A|p.Asp515Asn |
S47 |
7 | BAA05g22190 | A05 | 26399502 | C | T | synonymous_variant | LOW | c.1305G>A|p.Gln435Gln |
S35 |
8 | BAA05g22190 | A05 | 26400606 | G | A | missense_variant | MODERATE | c.298C>T|p.Leu100Phe |
S280 |
9 | BAA05g22190 | A05 | 26400744 | G | A | missense_variant | MODERATE | c.160C>T|p.Pro54Ser |
S120 |
10 | BAA05g22190 | A05 | 26403031 | C | T | upstream_gene_variant | MODIFIER | c.-2059G>A| |
S198 |
11 | BAA05g22190 | A05 | 26403060 | C | T | upstream_gene_variant | MODIFIER | c.-2088G>A| |
S57 |
12 | BAA05g22190 | A05 | 26403095 | G | A | upstream_gene_variant | MODIFIER | c.-2123C>T| |
S161 |