Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11360 | A01 | 5249242 | G | A | upstream_gene_variant | MODIFIER | c.-3891G>A| |
S287 |
2 | BAA01g11360 | A01 | 5250349 | G | T | upstream_gene_variant | MODIFIER | c.-2784G>T| |
S194 |
3 | BAA01g11360 | A01 | 5250622 | C | T | upstream_gene_variant | MODIFIER | c.-2511C>T| |
S130 |
4 | BAA01g11360 | A01 | 5250654 | G | A | upstream_gene_variant | MODIFIER | c.-2479G>A| |
S286 |
5 | BAA01g11360 | A01 | 5252329 | C | T | upstream_gene_variant | MODIFIER | c.-804C>T| |
S112 |
6 | BAA01g11360 | A01 | 5252687 | C | T | upstream_gene_variant | MODIFIER | c.-446C>T| |
S294 |
7 | BAA01g11360 | A01 | 5253337 | G | T | missense_variant&splice_region_variant | MODERATE | c.121G>T|p.Val41Leu |
S251 |
8 | BAA01g11360 | A01 | 5255430 | C | T | missense_variant | MODERATE | c.1283C>T|p.Ala428Val |
S192 |
9 | BAA01g11360 | A01 | 5255501 | C | T | missense_variant | MODERATE | c.1354C>T|p.His452Tyr |
S104 |
10 | BAA01g11360 | A01 | 5255600 | C | T | splice_region_variant&intron_variant | LOW | c.1369-4C>T| |
S151 |
11 | BAA01g11360 | A01 | 5256527 | C | T | downstream_gene_variant | MODIFIER | c.*697C>T| |
S36 |
12 | BAA01g11360 | A01 | 5259028 | G | A | downstream_gene_variant | MODIFIER | c.*3198G>A| |
S110 |
13 | BAA01g11360 | A01 | 5259558 | C | T | downstream_gene_variant | MODIFIER | c.*3728C>T| |
S136 |
14 | BAA01g11360 | A01 | 5260155 | G | A | downstream_gene_variant | MODIFIER | c.*4325G>A| |
S263 |