| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 135551 | BAA10g21400 | A10 | 18853636 | C | T | synonymous_variant | LOW | c.288C>T|p.Phe96Phe |
S51 |
| 135552 | BAA10g21410 | A10 | 18854019 | G | A | upstream_gene_variant | MODIFIER | c.-1266G>A| |
S167 |
| 135553 | BAA10g21410 | A10 | 18855308 | C | T | synonymous_variant | LOW | c.24C>T|p.Leu8Leu |
S133 |
| 135554 | BAA10g21410 | A10 | 18855310 | G | A | stop_gained | HIGH | c.26G>A|p.Trp9* |
S27 |
| 135555 | BAA10g21410 | A10 | 18855608 | C | T | synonymous_variant | LOW | c.324C>T|p.Phe108Phe |
S70 |
| 135556 | BAA10g21410 | A10 | 18857150 | G | A | stop_gained | HIGH | c.1866G>A|p.Trp622* |
S9 |
| 135557 | BAA10g21410 | A10 | 18857167 | C | T | missense_variant | MODERATE | c.1883C>T|p.Ala628Val |
S235 S89 |
| 135558 | BAA10g21420 | A10 | 18858479 | C | T | upstream_gene_variant | MODIFIER | c.-998C>T| |
S60 |
| 135559 | BAA10g21420 | A10 | 18858584 | C | T | upstream_gene_variant | MODIFIER | c.-893C>T| |
S206 S26 |
| 135560 | BAA10g21420 | A10 | 18858743 | G | A | upstream_gene_variant | MODIFIER | c.-734G>A| |
S28 |
| 135561 | BAA10g21420 | A10 | 18859465 | C | T | upstream_gene_variant | MODIFIER | c.-12C>T| |
S38 |
| 135562 | BAA10g21420 | A10 | 18859645 | C | T | synonymous_variant | LOW | c.69C>T|p.Thr23Thr |
S18 |
| 135563 | BAA10g21420 | A10 | 18859949 | C | T | missense_variant | MODERATE | c.373C>T|p.Pro125Ser |
S244 |
| 135564 | BAA10g21420 | A10 | 18860804 | C | T | missense_variant | MODERATE | c.862C>T|p.Leu288Phe |
S68 |
| 135565 | BAA10g21420 | A10 | 18860835 | C | T | missense_variant | MODERATE | c.893C>T|p.Ser298Phe |
S23 |
| 135566 | BAA10g21420 | A10 | 18861406 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1245-1G>A| |
S62 |
| 135567 | BAA10g21420 | A10 | 18861557 | C | T | synonymous_variant | LOW | c.1395C>T|p.Ile465Ile |
S122 |
| 135568 | BAA10g21420 | A10 | 18861733 | C | T | missense_variant | MODERATE | c.1483C>T|p.Leu495Phe |
S45 |
| 135569 | BAA10g21420 | A10 | 18861933 | C | T | synonymous_variant | LOW | c.1683C>T|p.Tyr561Tyr |
S19 |
| 135570 | BAA10g21430 | A10 | 18862350 | C | T | synonymous_variant | LOW | c.1146G>A|p.Glu382Glu |
S186 |
| 135571 | BAA10g21430 | A10 | 18862819 | G | A | missense_variant | MODERATE | c.779C>T|p.Pro260Leu |
S149 |
| 135572 | BAA10g21440 | A10 | 18862956 | G | A | upstream_gene_variant | MODIFIER | c.-4178G>A| |
S215 |
| 135573 | BAA10g21440 | A10 | 18863052 | G | A | upstream_gene_variant | MODIFIER | c.-4082G>A| |
S94 |
| 135574 | BAA10g21440 | A10 | 18863085 | C | T | upstream_gene_variant | MODIFIER | c.-4049C>T| |
S23 |
| 135575 | BAA10g21440 | A10 | 18863235 | G | A | upstream_gene_variant | MODIFIER | c.-3899G>A| |
S132 S137 S89 |