Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33470 | A02 | 28643028 | C | T | upstream_gene_variant | MODIFIER | c.-3807C>T| |
S252 |
2 | BAA02g33470 | A02 | 28643533 | G | A | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S293 |
3 | BAA02g33470 | A02 | 28647009 | G | A | missense_variant | MODERATE | c.175G>A|p.Glu59Lys |
S77 S82 |
4 | BAA02g33470 | A02 | 28647086 | C | T | synonymous_variant | LOW | c.252C>T|p.Leu84Leu |
S87 |
5 | BAA02g33470 | A02 | 28647219 | G | A | missense_variant | MODERATE | c.385G>A|p.Gly129Arg |
S219 S72 |
6 | BAA02g33470 | A02 | 28649068 | C | T | synonymous_variant | LOW | c.1944C>T|p.Ile648Ile |
S92 |
7 | BAA02g33470 | A02 | 28649070 | C | T | missense_variant | MODERATE | c.1946C>T|p.Pro649Leu |
S15 S3 |
8 | BAA02g33470 | A02 | 28649091 | G | A | missense_variant | MODERATE | c.1967G>A|p.Gly656Asp |
S126 |
9 | BAA02g33470 | A02 | 28649628 | C | T | missense_variant | MODERATE | c.2504C>T|p.Thr835Met |
S193 |
10 | BAA02g33470 | A02 | 28649669 | G | A | missense_variant | MODERATE | c.2545G>A|p.Gly849Arg |
S61 |
11 | BAA02g33470 | A02 | 28649915 | G | A | missense_variant | MODERATE | c.2723G>A|p.Ser908Asn |
S61 |
12 | BAA02g33470 | A02 | 28649994 | G | A | synonymous_variant | LOW | c.2802G>A|p.Leu934Leu |
S130 |
13 | BAA02g33470 | A02 | 28651510 | G | A | downstream_gene_variant | MODIFIER | c.*1114G>A| |
S186 |
14 | BAA02g33470 | A02 | 28652603 | G | A | downstream_gene_variant | MODIFIER | c.*2207G>A| |
S58 |
15 | BAA02g33470 | A02 | 28653919 | G | A | downstream_gene_variant | MODIFIER | c.*3523G>A| |
S302 |
16 | BAA02g33470 | A02 | 28654125 | C | T | downstream_gene_variant | MODIFIER | c.*3729C>T| |
S52 |
17 | BAA02g33470 | A02 | 28654163 | C | T | downstream_gene_variant | MODIFIER | c.*3767C>T| |
S54 |
18 | BAA02g33470 | A02 | 28655020 | C | T | downstream_gene_variant | MODIFIER | c.*4624C>T| |
S152 |
19 | BAA02g33470 | A02 | 28655112 | C | T | downstream_gene_variant | MODIFIER | c.*4716C>T| |
S260 |