| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 131751 | BAA10g18920 | A10 | 17541196 | G | A | missense_variant | MODERATE | c.461G>A|p.Arg154Lys |
S144 |
| 131752 | BAA10g18920 | A10 | 17541457 | G | A | stop_gained | HIGH | c.722G>A|p.Trp241* |
S64 |
| 131753 | BAA10g18910 | A10 | 17542602 | G | A | downstream_gene_variant | MODIFIER | c.*2961G>A| |
S155 S211 |
| 131754 | BAA10g18930 | A10 | 17542625 | C | T | splice_region_variant&synonymous_variant | LOW | c.747G>A|p.Lys249Lys |
S86 |
| 131755 | BAA10g18930 | A10 | 17543960 | G | A | upstream_gene_variant | MODIFIER | c.-189C>T| |
S9 |
| 131756 | BAA10g18940 | A10 | 17545221 | C | T | synonymous_variant | LOW | c.2103G>A|p.Ser701Ser |
S148 S30 S31 |
| 131757 | BAA10g18940 | A10 | 17546081 | G | A | missense_variant | MODERATE | c.1322C>T|p.Pro441Leu |
S94 |
| 131758 | BAA10g18930 | A10 | 17547632 | C | T | upstream_gene_variant | MODIFIER | c.-3861G>A| |
S190 |
| 131759 | BAA10g18940 | A10 | 17548011 | C | T | missense_variant | MODERATE | c.451G>A|p.Glu151Lys |
S186 |
| 131760 | BAA10g18930 | A10 | 17548547 | G | A | upstream_gene_variant | MODIFIER | c.-4776C>T| |
S149 |
| 131761 | BAA10g18940 | A10 | 17548773 | G | A | upstream_gene_variant | MODIFIER | c.-312C>T| |
S134 |
| 131762 | BAA10g18940 | A10 | 17548876 | C | T | upstream_gene_variant | MODIFIER | c.-415G>A| |
S221 |
| 131763 | BAA10g18940 | A10 | 17550230 | C | T | upstream_gene_variant | MODIFIER | c.-1769G>A| |
S259 |
| 131764 | BAA10g18940 | A10 | 17550342 | G | A | upstream_gene_variant | MODIFIER | c.-1881C>T| |
S38 |
| 131765 | BAA10g18940 | A10 | 17550568 | C | T | upstream_gene_variant | MODIFIER | c.-2107G>A| |
S61 |
| 131766 | BAA10g18940 | A10 | 17551382 | T | A | upstream_gene_variant | MODIFIER | c.-2921A>T| |
S244 |
| 131767 | BAA10g18940 | A10 | 17552722 | G | A | upstream_gene_variant | MODIFIER | c.-4261C>T| |
S105 S106 |
| 131768 | BAA10g18950 | A10 | 17552830 | C | T | missense_variant | MODERATE | c.1207G>A|p.Glu403Lys |
S45 |
| 131769 | BAA10g18950 | A10 | 17553134 | C | T | synonymous_variant | LOW | c.903G>A|p.Gly301Gly |
S169 |
| 131770 | BAA10g18950 | A10 | 17553167 | C | T | synonymous_variant | LOW | c.870G>A|p.Gln290Gln |
S191 |
| 131771 | BAA10g18950 | A10 | 17553619 | C | T | missense_variant | MODERATE | c.418G>A|p.Val140Ile |
S37 |
| 131772 | BAA10g18950 | A10 | 17555214 | C | T | upstream_gene_variant | MODIFIER | c.-1178G>A| |
S249 |
| 131773 | BAA10g18950 | A10 | 17555249 | C | T | upstream_gene_variant | MODIFIER | c.-1213G>A| |
S259 |
| 131774 | BAA10g18950 | A10 | 17555485 | C | T | upstream_gene_variant | MODIFIER | c.-1449G>A| |
S11 |
| 131775 | BAA10g18950 | A10 | 17556824 | G | A | upstream_gene_variant | MODIFIER | c.-2788C>T| |
S205 |