| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 16751 | BAA01g12690 | A01 | 5991871 | G | A | synonymous_variant | LOW | c.336G>A|p.Lys112Lys |
S28 |
| 16752 | BAA01g12690 | A01 | 5992485 | G | A | missense_variant | MODERATE | c.950G>A|p.Gly317Glu |
S257 |
| 16753 | BAA01g12690 | A01 | 5992566 | C | T | missense_variant | MODERATE | c.1031C>T|p.Thr344Ile |
S289 S290 |
| 16754 | BAA01g12690 | A01 | 5992665 | G | A | missense_variant | MODERATE | c.1130G>A|p.Gly377Glu |
S142 |
| 16755 | BAA01g12690 | A01 | 5992874 | C | T | missense_variant | MODERATE | c.1339C>T|p.Pro447Ser |
S136 |
| 16756 | BAA01g12690 | A01 | 5993592 | C | T | synonymous_variant | LOW | c.1671C>T|p.Ala557Ala |
S198 |
| 16757 | BAA01g12690 | A01 | 5993691 | C | T | downstream_gene_variant | MODIFIER | c.*63C>T| |
S135 |
| 16758 | BAA01g12690 | A01 | 5993707 | C | T | downstream_gene_variant | MODIFIER | c.*79C>T| |
S108 |
| 16759 | BAA01g12690 | A01 | 5995252 | C | T | downstream_gene_variant | MODIFIER | c.*1624C>T| |
S140 |
| 16760 | BAA01g12690 | A01 | 5995384 | C | T | downstream_gene_variant | MODIFIER | c.*1756C>T| |
S112 |
| 16761 | BAA01g12690 | A01 | 5996754 | G | A | downstream_gene_variant | MODIFIER | c.*3126G>A| |
S203 |
| 16762 | BAA01g12690 | A01 | 5997669 | C | T | downstream_gene_variant | MODIFIER | c.*4041C>T| |
S249 |
| 16763 | BAA01g12700 | A01 | 5997894 | G | A | missense_variant | MODERATE | c.3218C>T|p.Ser1073Phe |
S79 S91 |
| 16764 | BAA01g12700 | A01 | 5998173 | C | T | missense_variant | MODERATE | c.3113G>A|p.Gly1038Glu |
S210 S225 |
| 16765 | BAA01g12690 | A01 | 5998505 | G | A | downstream_gene_variant | MODIFIER | c.*4877G>A| |
S272 |
| 16766 | BAA01g12700 | A01 | 5999205 | G | A | synonymous_variant | LOW | c.2721C>T|p.Pro907Pro |
S247 |
| 16767 | BAA01g12700 | A01 | 5999963 | C | T | missense_variant | MODERATE | c.2491G>A|p.Gly831Ser |
S132 S137 S215 |
| 16768 | BAA01g12700 | A01 | 6000362 | G | A | missense_variant | MODERATE | c.2251C>T|p.Pro751Ser |
S302 S84 S93 |
| 16769 | BAA01g12700 | A01 | 6000405 | G | A | synonymous_variant | LOW | c.2208C>T|p.Ile736Ile |
S193 |
| 16770 | BAA01g12700 | A01 | 6000778 | G | A | intron_variant | MODIFIER | c.1954-44C>T| |
S122 |
| 16771 | BAA01g12700 | A01 | 6001492 | G | A | intron_variant | MODIFIER | c.1814+34C>T| |
S195 |
| 16772 | BAA01g12700 | A01 | 6002155 | C | T | missense_variant | MODERATE | c.1364G>A|p.Ser455Asn |
S48 |
| 16773 | BAA01g12700 | A01 | 6002250 | G | A | intron_variant | MODIFIER | c.1329+35C>T| |
S40 S49 |
| 16774 | BAA01g12700 | A01 | 6002807 | G | A | intron_variant | MODIFIER | c.1122+12C>T| |
S229 |
| 16775 | BAA01g12700 | A01 | 6003773 | G | A | missense_variant | MODERATE | c.587C>T|p.Pro196Leu |
S247 |