Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11800 | A01 | 5498063 | C | T | intron_variant | MODIFIER | c.499-347G>A| |
S164 |
2 | BAA01g11800 | A01 | 5499115 | G | A | splice_region_variant&intron_variant | LOW | c.465-4C>T| |
S235 |
3 | BAA01g11800 | A01 | 5500034 | C | T | intron_variant | MODIFIER | c.377-372G>A| |
S82 |
4 | BAA01g11800 | A01 | 5500270 | C | T | intron_variant | MODIFIER | c.377-608G>A| |
S219 S72 |
5 | BAA01g11800 | A01 | 5502863 | G | A | intron_variant | MODIFIER | c.376+2239C>T| |
S34 |
6 | BAA01g11800 | A01 | 5502966 | G | A | intron_variant | MODIFIER | c.376+2136C>T| |
S178 |
7 | BAA01g11800 | A01 | 5505736 | G | A | intron_variant | MODIFIER | c.293-551C>T| |
S133 |
8 | BAA01g11800 | A01 | 5507032 | G | A | intron_variant | MODIFIER | c.293-1847C>T| |
S281 |
9 | BAA01g11800 | A01 | 5509502 | G | A | intron_variant | MODIFIER | c.292+3664C>T| |
S184 |
10 | BAA01g11800 | A01 | 5510270 | G | A | intron_variant | MODIFIER | c.292+2896C>T| |
S142 |
11 | BAA01g11800 | A01 | 5510491 | G | A | intron_variant | MODIFIER | c.292+2675C>T| |
S191 |
12 | BAA01g11800 | A01 | 5510537 | C | T | intron_variant | MODIFIER | c.292+2629G>A| |
S4 |
13 | BAA01g11800 | A01 | 5510553 | G | A | intron_variant | MODIFIER | c.292+2613C>T| |
S110 |
14 | BAA01g11800 | A01 | 5510841 | C | T | intron_variant | MODIFIER | c.292+2325G>A| |
S112 |
15 | BAA01g11800 | A01 | 5513185 | G | A | synonymous_variant | LOW | c.273C>T|p.Tyr91Tyr |
S173 |
16 | BAA01g11800 | A01 | 5513804 | G | A | upstream_gene_variant | MODIFIER | c.-347C>T| |
S67 |
17 | BAA01g11800 | A01 | 5513928 | G | A | upstream_gene_variant | MODIFIER | c.-471C>T| |
S105 S106 |
18 | BAA01g11800 | A01 | 5515512 | C | T | upstream_gene_variant | MODIFIER | c.-2055G>A| |
S299 |