Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13460 | A08 | 11664861 | C | T | upstream_gene_variant | MODIFIER | c.-3418C>T| |
S196 |
2 | BAA08g13460 | A08 | 11666047 | G | A | upstream_gene_variant | MODIFIER | c.-2232G>A| |
S190 |
3 | BAA08g13460 | A08 | 11666162 | C | T | upstream_gene_variant | MODIFIER | c.-2117C>T| |
S230 |
4 | BAA08g13460 | A08 | 11668042 | G | A | upstream_gene_variant | MODIFIER | c.-237G>A| |
S81 S85 |
5 | BAA08g13460 | A08 | 11668675 | C | T | missense_variant | MODERATE | c.397C>T|p.Pro133Ser |
S58 |
6 | BAA08g13460 | A08 | 11668781 | G | A | missense_variant | MODERATE | c.503G>A|p.Arg168His |
S92 |
7 | BAA08g13460 | A08 | 11668918 | G | A | missense_variant | MODERATE | c.640G>A|p.Gly214Arg |
S299 |
8 | BAA08g13460 | A08 | 11669310 | C | T | synonymous_variant | LOW | c.1032C>T|p.Ile344Ile |
S80 |
9 | BAA08g13460 | A08 | 11669695 | G | A | missense_variant | MODERATE | c.1417G>A|p.Gly473Arg |
S87 |
10 | BAA08g13460 | A08 | 11669861 | C | T | missense_variant | MODERATE | c.1583C>T|p.Pro528Leu |
S208 S219 |
11 | BAA08g13460 | A08 | 11670145 | G | A | downstream_gene_variant | MODIFIER | c.*85G>A| |
S111 |
12 | BAA08g13460 | A08 | 11670214 | C | T | downstream_gene_variant | MODIFIER | c.*154C>T| |
S206 S26 |
13 | BAA08g13460 | A08 | 11670487 | G | A | downstream_gene_variant | MODIFIER | c.*427G>A| |
S221 |
14 | BAA08g13460 | A08 | 11670990 | G | A | downstream_gene_variant | MODIFIER | c.*930G>A| |
S157 S163 |
15 | BAA08g13460 | A08 | 11671569 | G | A | downstream_gene_variant | MODIFIER | c.*1509G>A| |
S200 |
16 | BAA08g13460 | A08 | 11672193 | G | A | downstream_gene_variant | MODIFIER | c.*2133G>A| |
S46 |