Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13200 | A08 | 11450458 | G | A | stop_gained | HIGH | c.195G>A|p.Trp65* |
S257 |
2 | BAA08g13200 | A08 | 11451317 | C | T | missense_variant | MODERATE | c.1054C>T|p.Leu352Phe |
S208 |
3 | BAA08g13200 | A08 | 11451539 | G | A | missense_variant | MODERATE | c.1276G>A|p.Asp426Asn |
S96 |
4 | BAA08g13200 | A08 | 11452112 | G | A | missense_variant | MODERATE | c.1849G>A|p.Asp617Asn |
S47 |
5 | BAA08g13200 | A08 | 11452144 | C | T | synonymous_variant | LOW | c.1881C>T|p.Ile627Ile |
S89 |
6 | BAA08g13200 | A08 | 11453702 | G | A | downstream_gene_variant | MODIFIER | c.*1090G>A| |
S185 |
7 | BAA08g13200 | A08 | 11453993 | C | T | downstream_gene_variant | MODIFIER | c.*1381C>T| |
S130 |
8 | BAA08g13200 | A08 | 11454317 | C | T | downstream_gene_variant | MODIFIER | c.*1705C>T| |
S17 |
9 | BAA08g13200 | A08 | 11454361 | C | T | downstream_gene_variant | MODIFIER | c.*1749C>T| |
S152 |
10 | BAA08g13200 | A08 | 11454713 | C | T | downstream_gene_variant | MODIFIER | c.*2101C>T| |
S166 S233 |
11 | BAA08g13200 | A08 | 11454748 | G | A | downstream_gene_variant | MODIFIER | c.*2136G>A| |
S187 |
12 | BAA08g13200 | A08 | 11455032 | C | T | downstream_gene_variant | MODIFIER | c.*2420C>T| |
S249 |
13 | BAA08g13200 | A08 | 11455526 | C | T | downstream_gene_variant | MODIFIER | c.*2914C>T| |
S178 |
14 | BAA08g13200 | A08 | 11455842 | C | T | downstream_gene_variant | MODIFIER | c.*3230C>T| |
S249 |
15 | BAA08g13200 | A08 | 11456061 | C | T | downstream_gene_variant | MODIFIER | c.*3449C>T| |
S76 |