| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 79651 | BAA01g41890 | A01 | 27865295 | G | A | missense_variant | MODERATE | c.580G>A|p.Gly194Arg |
S152 |
| 79652 | BAA01g41900 | A01 | 27867547 | G | A | synonymous_variant | LOW | c.2622C>T|p.Val874Val |
S144 |
| 79653 | BAA01g41900 | A01 | 27867781 | G | A | synonymous_variant | LOW | c.2388C>T|p.Phe796Phe |
S272 |
| 79654 | BAA01g41900 | A01 | 27867807 | G | A | missense_variant | MODERATE | c.2362C>T|p.Pro788Ser |
S262 |
| 79655 | BAA01g41900 | A01 | 27867957 | C | T | missense_variant | MODERATE | c.2212G>A|p.Glu738Lys |
S255 |
| 79656 | BAA01g41900 | A01 | 27868925 | G | A | missense_variant | MODERATE | c.1244C>T|p.Ser415Leu |
S251 |
| 79657 | BAA01g41900 | A01 | 27869902 | C | T | stop_gained | HIGH | c.267G>A|p.Trp89* |
S156 |
| 79658 | BAA01g41900 | A01 | 27871286 | C | T | upstream_gene_variant | MODIFIER | c.-1118G>A| |
S155 S211 |
| 79659 | BAA01g41910 | A01 | 27871503 | C | T | missense_variant | MODERATE | c.1165G>A|p.Glu389Lys |
S133 |
| 79660 | BAA01g41910 | A01 | 27871543 | C | T | stop_gained | HIGH | c.1125G>A|p.Trp375* |
S50 |
| 79661 | BAA01g41910 | A01 | 27873298 | C | T | missense_variant | MODERATE | c.16G>A|p.Glu6Lys |
S74 |
| 79662 | BAA01g41900 | A01 | 27873397 | C | T | upstream_gene_variant | MODIFIER | c.-3229G>A| |
S153 |
| 79663 | BAA01g41920 | A01 | 27880516 | G | A | downstream_gene_variant | MODIFIER | c.*3049C>T| |
S225 S73 |
| 79664 | BAA01g41920 | A01 | 27880708 | G | A | downstream_gene_variant | MODIFIER | c.*2857C>T| |
S176 |
| 79665 | BAA01g41920 | A01 | 27880728 | G | A | downstream_gene_variant | MODIFIER | c.*2837C>T| |
S244 |
| 79666 | BAA01g41920 | A01 | 27880845 | G | A | downstream_gene_variant | MODIFIER | c.*2720C>T| |
S225 |
| 79667 | BAA01g41920 | A01 | 27881105 | G | A | downstream_gene_variant | MODIFIER | c.*2460C>T| |
S268 |
| 79668 | BAA01g41920 | A01 | 27881590 | C | T | downstream_gene_variant | MODIFIER | c.*1975G>A| |
S40 S49 |
| 79669 | BAA01g41920 | A01 | 27883901 | G | A | synonymous_variant | LOW | c.2454C>T|p.Phe818Phe |
S140 S219 S279 S72 |
| 79670 | BAA01g41920 | A01 | 27884074 | G | A | synonymous_variant | LOW | c.2281C>T|p.Leu761Leu |
S268 |
| 79671 | BAA01g41920 | A01 | 27884185 | C | T | missense_variant | MODERATE | c.2170G>A|p.Val724Met |
S288 |
| 79672 | BAA01g41920 | A01 | 27884284 | C | T | missense_variant | MODERATE | c.2071G>A|p.Asp691Asn |
S59 |
| 79673 | BAA01g41920 | A01 | 27885155 | C | T | synonymous_variant | LOW | c.1200G>A|p.Lys400Lys |
S183 |
| 79674 | BAA01g41920 | A01 | 27886276 | C | T | missense_variant | MODERATE | c.79G>A|p.Asp27Asn |
S54 |
| 79675 | BAA01g41930 | A01 | 27887565 | G | A | synonymous_variant | LOW | c.2130C>T|p.Leu710Leu |
S84 S93 |