| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 119201 | BAA10g11370 | A10 | 12946496 | G | A | downstream_gene_variant | MODIFIER | c.*202G>A| |
S203 |
| 119202 | BAA10g11370 | A10 | 12949064 | C | T | downstream_gene_variant | MODIFIER | c.*2770C>T| |
S99 |
| 119203 | BAA10g11370 | A10 | 12949366 | C | T | downstream_gene_variant | MODIFIER | c.*3072C>T| |
S210 S225 |
| 119204 | BAA10g11370 | A10 | 12949419 | G | A | downstream_gene_variant | MODIFIER | c.*3125G>A| |
S202 |
| 119205 | BAA10g11370 | A10 | 12949804 | G | A | downstream_gene_variant | MODIFIER | c.*3510G>A| |
S302 |
| 119206 | BAA10g11370 | A10 | 12949809 | G | A | downstream_gene_variant | MODIFIER | c.*3515G>A| |
S77 S82 |
| 119207 | BAA10g11370 | A10 | 12950052 | C | T | downstream_gene_variant | MODIFIER | c.*3758C>T| |
S99 |
| 119208 | BAA10g11370 | A10 | 12950384 | G | A | downstream_gene_variant | MODIFIER | c.*4090G>A| |
S202 |
| 119209 | BAA10g11380 | A10 | 12951390 | C | T | downstream_gene_variant | MODIFIER | c.*4441G>A| |
S142 |
| 119210 | BAA10g11380 | A10 | 12951462 | C | T | downstream_gene_variant | MODIFIER | c.*4369G>A| |
S47 |
| 119211 | BAA10g11380 | A10 | 12952085 | G | A | downstream_gene_variant | MODIFIER | c.*3746C>T| |
S18 |
| 119212 | BAA10g11380 | A10 | 12952289 | C | T | downstream_gene_variant | MODIFIER | c.*3542G>A| |
S269 |
| 119213 | BAA10g11380 | A10 | 12955268 | C | T | downstream_gene_variant | MODIFIER | c.*563G>A| |
S308 |
| 119214 | BAA10g11380 | A10 | 12955457 | G | A | downstream_gene_variant | MODIFIER | c.*374C>T| |
S95 |
| 119215 | BAA10g11390 | A10 | 12956201 | C | A | upstream_gene_variant | MODIFIER | c.-4401C>A| |
S231 |
| 119216 | BAA10g11380 | A10 | 12956685 | G | A | missense_variant | MODERATE | c.277C>T|p.Pro93Ser |
S178 |
| 119217 | BAA10g11380 | A10 | 12956858 | C | T | missense_variant | MODERATE | c.104G>A|p.Cys35Tyr |
S28 |
| 119218 | BAA10g11380 | A10 | 12956874 | G | A | missense_variant | MODERATE | c.88C>T|p.Arg30Cys |
S114 S280 |
| 119219 | BAA10g11380 | A10 | 12957849 | C | T | upstream_gene_variant | MODIFIER | c.-888G>A| |
S131 |
| 119220 | BAA10g11380 | A10 | 12959955 | C | T | upstream_gene_variant | MODIFIER | c.-2994G>A| |
S188 |
| 119221 | BAA10g11390 | A10 | 12960611 | C | T | synonymous_variant | LOW | c.10C>T|p.Leu4Leu |
S63 |
| 119222 | BAA10g11410 | A10 | 12967829 | G | A | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S71 S85 |
| 119223 | BAA10g11410 | A10 | 12968381 | C | T | upstream_gene_variant | MODIFIER | c.-2146C>T| |
S210 S225 |
| 119224 | BAA10g11410 | A10 | 12968892 | G | A | upstream_gene_variant | MODIFIER | c.-1635G>A| |
S155 S211 |
| 119225 | BAA10g11410 | A10 | 12969641 | C | T | upstream_gene_variant | MODIFIER | c.-886C>T| |
S117 |