| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150601 | BAA10g34550 | A10 | 24262667 | C | T | synonymous_variant | LOW | c.198G>A|p.Ala66Ala |
S80 |
| 150602 | BAA10g34540 | A10 | 24263255 | G | A | upstream_gene_variant | MODIFIER | c.-1963C>T| |
S308 |
| 150603 | BAA10g34540 | A10 | 24263365 | C | T | upstream_gene_variant | MODIFIER | c.-2073G>A| |
S292 |
| 150604 | BAA10g34540 | A10 | 24263610 | G | A | upstream_gene_variant | MODIFIER | c.-2318C>T| |
S203 |
| 150605 | BAA10g34560 | A10 | 24264090 | C | T | missense_variant&splice_region_variant | MODERATE | c.847G>A|p.Val283Ile |
S47 |
| 150606 | BAA10g34560 | A10 | 24264189 | G | A | missense_variant | MODERATE | c.832C>T|p.Leu278Phe |
S303 |
| 150607 | BAA10g34560 | A10 | 24264399 | C | T | missense_variant | MODERATE | c.712G>A|p.Val238Met |
S33 |
| 150608 | BAA10g34540 | A10 | 24265421 | G | A | upstream_gene_variant | MODIFIER | c.-4129C>T| |
S139 |
| 150609 | BAA10g34560 | A10 | 24268073 | C | T | upstream_gene_variant | MODIFIER | c.-2085G>A| |
S204 |
| 150610 | BAA10g34560 | A10 | 24268734 | C | T | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S170 |
| 150611 | BAA10g34560 | A10 | 24269923 | C | T | upstream_gene_variant | MODIFIER | c.-3935G>A| |
S292 |
| 150612 | BAA10g34570 | A10 | 24271636 | G | A | upstream_gene_variant | MODIFIER | c.-2623G>A| |
S276 |
| 150613 | BAA10g34570 | A10 | 24271729 | C | T | upstream_gene_variant | MODIFIER | c.-2530C>T| |
S110 |
| 150614 | BAA10g34570 | A10 | 24272295 | C | T | upstream_gene_variant | MODIFIER | c.-1964C>T| |
S174 S39 |
| 150615 | BAA10g34570 | A10 | 24273378 | C | T | upstream_gene_variant | MODIFIER | c.-881C>T| |
S18 |
| 150616 | BAA10g34570 | A10 | 24273705 | G | A | upstream_gene_variant | MODIFIER | c.-554G>A| |
S59 |
| 150617 | BAA10g34570 | A10 | 24274002 | A | C | upstream_gene_variant | MODIFIER | c.-257A>C| |
S119 S186 S198 S232 S256 S291 S306 |
| 150618 | BAA10g34570 | A10 | 24274457 | C | T | missense_variant | MODERATE | c.199C>T|p.Pro67Ser |
S157 |
| 150619 | BAA10g34570 | A10 | 24274703 | A | C | downstream_gene_variant | MODIFIER | c.*223A>C| |
S149 S174 S283 S291 S295 S5 |
| 150620 | BAA10g34590 | A10 | 24277311 | G | A | missense_variant | MODERATE | c.1628C>T|p.Ala543Val |
S4 |
| 150621 | BAA10g34580 | A10 | 24277743 | C | T | upstream_gene_variant | MODIFIER | c.-1510G>A| |
S277 |
| 150622 | BAA10g34600 | A10 | 24281534 | G | A | synonymous_variant | LOW | c.243C>T|p.Leu81Leu |
S212 |
| 150623 | BAA10g34600 | A10 | 24281691 | C | T | stop_gained | HIGH | c.86G>A|p.Trp29* |
S108 |
| 150624 | BAA10g34610 | A10 | 24282557 | G | A | missense_variant | MODERATE | c.220C>T|p.Arg74Cys |
S250 |
| 150625 | BAA10g34590 | A10 | 24283347 | G | A | upstream_gene_variant | MODIFIER | c.-3393C>T| |
S299 |