Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00490 | A10 | 226767 | G | A | downstream_gene_variant | MODIFIER | c.*1267C>T| |
S83 S88 |
2 | BAA10g00490 | A10 | 228817 | C | T | synonymous_variant | LOW | c.1431G>A|p.Glu477Glu |
S260 |
3 | BAA10g00490 | A10 | 229149 | G | A | missense_variant | MODERATE | c.1099C>T|p.Pro367Ser |
S197 |
4 | BAA10g00490 | A10 | 230094 | G | A | synonymous_variant | LOW | c.414C>T|p.Leu138Leu |
S126 |
5 | BAA10g00490 | A10 | 232955 | G | A | upstream_gene_variant | MODIFIER | c.-2448C>T| |
S45 |
6 | BAA10g00490 | A10 | 233729 | G | A | upstream_gene_variant | MODIFIER | c.-3222C>T| |
S295 |
7 | BAA10g00490 | A10 | 234424 | C | T | upstream_gene_variant | MODIFIER | c.-3917G>A| |
S233 |
8 | BAA10g00490 | A10 | 234750 | C | T | upstream_gene_variant | MODIFIER | c.-4243G>A| |
S261 |
9 | BAA10g00490 | A10 | 234993 | G | A | upstream_gene_variant | MODIFIER | c.-4486C>T| |
S62 |
10 | BAA10g00490 | A10 | 235242 | C | T | upstream_gene_variant | MODIFIER | c.-4735G>A| |
S270 |
11 | BAA10g00490 | A10 | 235320 | G | A | upstream_gene_variant | MODIFIER | c.-4813C>T| |
S128 |