Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12760 | A01 | 6034815 | C | T | intron_variant | MODIFIER | c.2235+2861G>A| |
S151 S263 |
2 | BAA01g12760 | A01 | 6035106 | G | A | intron_variant | MODIFIER | c.2235+2570C>T| |
S116 |
3 | BAA01g12760 | A01 | 6035261 | C | T | intron_variant | MODIFIER | c.2235+2415G>A| |
S296 |
4 | BAA01g12760 | A01 | 6035393 | C | T | intron_variant | MODIFIER | c.2235+2283G>A| |
S261 |
5 | BAA01g12760 | A01 | 6035517 | C | T | intron_variant | MODIFIER | c.2235+2159G>A| |
S79 S84 |
6 | BAA01g12760 | A01 | 6035887 | C | T | intron_variant | MODIFIER | c.2235+1789G>A| |
S169 |
7 | BAA01g12760 | A01 | 6035891 | G | A | intron_variant | MODIFIER | c.2235+1785C>T| |
S281 |
8 | BAA01g12760 | A01 | 6036153 | C | T | intron_variant | MODIFIER | c.2235+1523G>A| |
S135 |
9 | BAA01g12760 | A01 | 6036277 | G | A | intron_variant | MODIFIER | c.2235+1399C>T| |
S234 |
10 | BAA01g12760 | A01 | 6038324 | G | A | missense_variant | MODERATE | c.1769C>T|p.Ser590Leu |
S183 S198 |
11 | BAA01g12760 | A01 | 6038700 | C | T | missense_variant | MODERATE | c.1393G>A|p.Glu465Lys |
S192 |
12 | BAA01g12760 | A01 | 6038957 | C | T | missense_variant | MODERATE | c.1136G>A|p.Arg379Lys |
S112 S115 |
13 | BAA01g12760 | A01 | 6040672 | G | A | upstream_gene_variant | MODIFIER | c.-280C>T| |
S17 |
14 | BAA01g12760 | A01 | 6044092 | C | T | upstream_gene_variant | MODIFIER | c.-3700G>A| |
S260 |
15 | BAA01g12760 | A01 | 6044325 | C | T | upstream_gene_variant | MODIFIER | c.-3933G>A| |
S289 S290 |