| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g06970 | A10 | 3745444 | C | T | downstream_gene_variant | MODIFIER | c.*4692G>A| |
S200 |
| 2 | BAA10g06970 | A10 | 3745525 | G | A | downstream_gene_variant | MODIFIER | c.*4611C>T| |
S48 |
| 3 | BAA10g06970 | A10 | 3745589 | G | A | downstream_gene_variant | MODIFIER | c.*4547C>T| |
S303 |
| 4 | BAA10g06970 | A10 | 3745605 | C | T | downstream_gene_variant | MODIFIER | c.*4531G>A| |
S259 |
| 5 | BAA10g06970 | A10 | 3745899 | C | T | downstream_gene_variant | MODIFIER | c.*4237G>A| |
S44 |
| 6 | BAA10g06970 | A10 | 3746059 | C | T | downstream_gene_variant | MODIFIER | c.*4077G>A| |
S35 |
| 7 | BAA10g06970 | A10 | 3746642 | G | A | downstream_gene_variant | MODIFIER | c.*3494C>T| |
S215 |
| 8 | BAA10g06970 | A10 | 3746979 | G | A | downstream_gene_variant | MODIFIER | c.*3157C>T| |
S64 |
| 9 | BAA10g06970 | A10 | 3747089 | G | A | downstream_gene_variant | MODIFIER | c.*3047C>T| |
S291 |
| 10 | BAA10g06970 | A10 | 3747280 | G | A | downstream_gene_variant | MODIFIER | c.*2856C>T| |
S13 |
| 11 | BAA10g06970 | A10 | 3747381 | C | T | downstream_gene_variant | MODIFIER | c.*2755G>A| |
S10 |
| 12 | BAA10g06970 | A10 | 3747808 | C | T | downstream_gene_variant | MODIFIER | c.*2328G>A| |
S249 |
| 13 | BAA10g06970 | A10 | 3748421 | G | A | downstream_gene_variant | MODIFIER | c.*1715C>T| |
S240 |
| 14 | BAA10g06970 | A10 | 3749040 | C | T | downstream_gene_variant | MODIFIER | c.*1096G>A| |
S159 S187 S243 S298 S299 |
| 15 | BAA10g06970 | A10 | 3749624 | C | T | downstream_gene_variant | MODIFIER | c.*512G>A| |
S15 S156 S2 S3 S34 |
| 16 | BAA10g06970 | A10 | 3750590 | G | A | intron_variant | MODIFIER | c.295-21C>T| |
S105 S106 |
| 17 | BAA10g06970 | A10 | 3750695 | G | A | missense_variant | MODERATE | c.256C>T|p.Pro86Ser |
S138 |
| 18 | BAA10g06970 | A10 | 3750868 | G | A | intron_variant | MODIFIER | c.136-53C>T| |
S46 |
| 19 | BAA10g06970 | A10 | 3751599 | G | A | missense_variant | MODERATE | c.116C>T|p.Pro39Leu |
S230 |
| 20 | BAA10g06970 | A10 | 3752052 | C | T | upstream_gene_variant | MODIFIER | c.-338G>A| |
S37 |
| 21 | BAA10g06970 | A10 | 3752641 | G | A | upstream_gene_variant | MODIFIER | c.-927C>T| |
S293 |
| 22 | BAA10g06970 | A10 | 3752711 | G | A | upstream_gene_variant | MODIFIER | c.-997C>T| |
S136 |
| 23 | BAA10g06970 | A10 | 3753312 | G | A | upstream_gene_variant | MODIFIER | c.-1598C>T| |
S251 |
| 24 | BAA10g06970 | A10 | 3753759 | C | T | upstream_gene_variant | MODIFIER | c.-2045G>A| |
S170 |
| 25 | BAA10g06970 | A10 | 3754060 | C | T | upstream_gene_variant | MODIFIER | c.-2346G>A| |
S117 |