Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23700 | A10 | 19827245 | G | T | missense_variant | MODERATE | c.491C>A|p.Ser164Tyr |
S116 |
2 | BAA10g23700 | A10 | 19827740 | C | T | upstream_gene_variant | MODIFIER | c.-5G>A| |
S97 |
3 | BAA10g23700 | A10 | 19828590 | C | T | upstream_gene_variant | MODIFIER | c.-855G>A| |
S142 |
4 | BAA10g23700 | A10 | 19828620 | C | T | upstream_gene_variant | MODIFIER | c.-885G>A| |
S37 |
5 | BAA10g23700 | A10 | 19828941 | G | A | upstream_gene_variant | MODIFIER | c.-1206C>T| |
S180 |
6 | BAA10g23700 | A10 | 19828971 | G | A | upstream_gene_variant | MODIFIER | c.-1236C>T| |
S233 |
7 | BAA10g23700 | A10 | 19829127 | G | A | upstream_gene_variant | MODIFIER | c.-1392C>T| |
S89 |
8 | BAA10g23700 | A10 | 19829176 | G | A | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S69 |
9 | BAA10g23700 | A10 | 19829239 | C | T | upstream_gene_variant | MODIFIER | c.-1504G>A| |
S221 |
10 | BAA10g23700 | A10 | 19830000 | G | A | upstream_gene_variant | MODIFIER | c.-2265C>T| |
S127 |