Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48610 | A09 | 52364387 | C | T | upstream_gene_variant | MODIFIER | c.-574C>T| |
S118 |
2 | BAA09g48610 | A09 | 52365224 | C | T | synonymous_variant | LOW | c.264C>T|p.Thr88Thr |
S211 S227 |
3 | BAA09g48610 | A09 | 52365261 | G | A | missense_variant | MODERATE | c.301G>A|p.Val101Ile |
S291 |
4 | BAA09g48610 | A09 | 52365465 | G | A | missense_variant | MODERATE | c.505G>A|p.Val169Met |
S262 |
5 | BAA09g48610 | A09 | 52365532 | C | T | missense_variant | MODERATE | c.572C>T|p.Ser191Leu |
S208 |
6 | BAA09g48610 | A09 | 52365585 | G | A | missense_variant | MODERATE | c.625G>A|p.Glu209Lys |
S236 |
7 | BAA09g48610 | A09 | 52365652 | G | A | missense_variant | MODERATE | c.692G>A|p.Gly231Glu |
S172 S217 |
8 | BAA09g48610 | A09 | 52365660 | G | A | missense_variant | MODERATE | c.700G>A|p.Glu234Lys |
S149 |
9 | BAA09g48610 | A09 | 52365894 | G | A | missense_variant | MODERATE | c.934G>A|p.Glu312Lys |
S4 |
10 | BAA09g48610 | A09 | 52366103 | C | T | downstream_gene_variant | MODIFIER | c.*141C>T| |
S245 |
11 | BAA09g48610 | A09 | 52367344 | C | T | downstream_gene_variant | MODIFIER | c.*1382C>T| |
S267 |
12 | BAA09g48610 | A09 | 52367724 | C | T | downstream_gene_variant | MODIFIER | c.*1762C>T| |
S199 |
13 | BAA09g48610 | A09 | 52368225 | G | A | downstream_gene_variant | MODIFIER | c.*2263G>A| |
S112 |
14 | BAA09g48610 | A09 | 52368618 | G | A | downstream_gene_variant | MODIFIER | c.*2656G>A| |
S46 |
15 | BAA09g48610 | A09 | 52368778 | G | A | downstream_gene_variant | MODIFIER | c.*2816G>A| |
S110 |
16 | BAA09g48610 | A09 | 52369024 | C | T | downstream_gene_variant | MODIFIER | c.*3062C>T| |
S256 |
17 | BAA09g48610 | A09 | 52369328 | G | A | downstream_gene_variant | MODIFIER | c.*3366G>A| |
S197 |
18 | BAA09g48610 | A09 | 52369582 | G | A | downstream_gene_variant | MODIFIER | c.*3620G>A| |
S234 |