Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27590 | A08 | 19375580 | C | T | downstream_gene_variant | MODIFIER | c.*3798G>A| |
S162 |
2 | BAA08g27590 | A08 | 19376398 | C | T | downstream_gene_variant | MODIFIER | c.*2980G>A| |
S192 |
3 | BAA08g27590 | A08 | 19377739 | G | A | downstream_gene_variant | MODIFIER | c.*1639C>T| |
S128 |
4 | BAA08g27590 | A08 | 19379984 | G | A | synonymous_variant | LOW | c.1854C>T|p.Arg618Arg |
S54 |
5 | BAA08g27590 | A08 | 19380394 | G | A | synonymous_variant | LOW | c.1612C>T|p.Leu538Leu |
S79 S91 |
6 | BAA08g27590 | A08 | 19381278 | G | A | synonymous_variant | LOW | c.1173C>T|p.Phe391Phe |
S40 S49 |
7 | BAA08g27590 | A08 | 19381308 | C | T | synonymous_variant | LOW | c.1143G>A|p.Lys381Lys |
S157 |
8 | BAA08g27590 | A08 | 19381462 | C | T | intron_variant | MODIFIER | c.1040+21G>A| |
S213 |
9 | BAA08g27590 | A08 | 19381756 | G | A | missense_variant | MODERATE | c.767C>T|p.Ser256Leu |
S139 |
10 | BAA08g27590 | A08 | 19381881 | C | T | synonymous_variant | LOW | c.642G>A|p.Gly214Gly |
S262 |
11 | BAA08g27590 | A08 | 19381941 | C | T | synonymous_variant | LOW | c.582G>A|p.Val194Val |
S296 |
12 | BAA08g27590 | A08 | 19382256 | C | T | synonymous_variant | LOW | c.267G>A|p.Glu89Glu |
S152 |
13 | BAA08g27590 | A08 | 19382600 | C | T | upstream_gene_variant | MODIFIER | c.-78G>A| |
S243 |
14 | BAA08g27590 | A08 | 19385234 | C | T | upstream_gene_variant | MODIFIER | c.-2712G>A| |
S243 |
15 | BAA08g27590 | A08 | 19386360 | G | A | upstream_gene_variant | MODIFIER | c.-3838C>T| |
S301 S304 |
16 | BAA08g27590 | A08 | 19386409 | C | T | upstream_gene_variant | MODIFIER | c.-3887G>A| |
S59 |