Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12250 | A01 | 5753325 | G | A | upstream_gene_variant | MODIFIER | c.-3466G>A| |
S180 |
2 | BAA01g12250 | A01 | 5753642 | C | T | upstream_gene_variant | MODIFIER | c.-3149C>T| |
S192 |
3 | BAA01g12250 | A01 | 5754531 | G | T | upstream_gene_variant | MODIFIER | c.-2260G>T| |
S92 |
4 | BAA01g12250 | A01 | 5754567 | G | A | upstream_gene_variant | MODIFIER | c.-2224G>A| |
S178 |
5 | BAA01g12250 | A01 | 5754765 | C | T | upstream_gene_variant | MODIFIER | c.-2026C>T| |
S295 |
6 | BAA01g12250 | A01 | 5754804 | A | T | upstream_gene_variant | MODIFIER | c.-1987A>T| |
S32 |
7 | BAA01g12250 | A01 | 5755217 | C | T | upstream_gene_variant | MODIFIER | c.-1574C>T| |
S165 |
8 | BAA01g12250 | A01 | 5755336 | G | A | upstream_gene_variant | MODIFIER | c.-1455G>A| |
S172 |
9 | BAA01g12250 | A01 | 5755738 | C | T | upstream_gene_variant | MODIFIER | c.-1053C>T| |
S200 |
10 | BAA01g12250 | A01 | 5756912 | G | A | missense_variant | MODERATE | c.122G>A|p.Gly41Asp |
S201 |
11 | BAA01g12250 | A01 | 5756975 | C | T | missense_variant | MODERATE | c.185C>T|p.Pro62Leu |
S78 |
12 | BAA01g12250 | A01 | 5757032 | C | T | missense_variant | MODERATE | c.242C>T|p.Thr81Ile |
S211 |
13 | BAA01g12250 | A01 | 5757073 | C | T | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S58 |