Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17780 | A01 | 8641584 | C | T | downstream_gene_variant | MODIFIER | c.*4227G>A| |
S99 |
2 | BAA01g17780 | A01 | 8642483 | C | T | downstream_gene_variant | MODIFIER | c.*3328G>A| |
S146 |
3 | BAA01g17780 | A01 | 8643210 | C | T | downstream_gene_variant | MODIFIER | c.*2601G>A| |
S70 |
4 | BAA01g17780 | A01 | 8643561 | C | T | downstream_gene_variant | MODIFIER | c.*2250G>A| |
S284 |
5 | BAA01g17780 | A01 | 8644011 | C | T | downstream_gene_variant | MODIFIER | c.*1800G>A| |
S47 |
6 | BAA01g17780 | A01 | 8644211 | C | T | downstream_gene_variant | MODIFIER | c.*1600G>A| |
S88 |
7 | BAA01g17780 | A01 | 8644928 | C | T | downstream_gene_variant | MODIFIER | c.*883G>A| |
S179 |
8 | BAA01g17780 | A01 | 8644963 | G | A | downstream_gene_variant | MODIFIER | c.*848C>T| |
S195 |
9 | BAA01g17780 | A01 | 8644970 | G | A | downstream_gene_variant | MODIFIER | c.*841C>T| |
S262 |
10 | BAA01g17780 | A01 | 8646609 | C | T | missense_variant | MODERATE | c.721G>A|p.Ala241Thr |
S40 S49 |
11 | BAA01g17780 | A01 | 8647237 | G | A | missense_variant | MODERATE | c.490C>T|p.Leu164Phe |
S178 |
12 | BAA01g17780 | A01 | 8647352 | C | T | synonymous_variant | LOW | c.375G>A|p.Lys125Lys |
S88 |
13 | BAA01g17780 | A01 | 8647364 | G | A | synonymous_variant | LOW | c.363C>T|p.Ile121Ile |
S94 |
14 | BAA01g17780 | A01 | 8647511 | C | T | missense_variant | MODERATE | c.292G>A|p.Gly98Arg |
S51 |
15 | BAA01g17780 | A01 | 8648668 | G | A | upstream_gene_variant | MODIFIER | c.-866C>T| |
S84 S93 |
16 | BAA01g17780 | A01 | 8649663 | C | T | upstream_gene_variant | MODIFIER | c.-1861G>A| |
S255 |
17 | BAA01g17780 | A01 | 8651533 | G | A | upstream_gene_variant | MODIFIER | c.-3731C>T| |
S172 S217 |