| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 76651 | BAA01g40500 | A01 | 26826013 | G | A | missense_variant | MODERATE | c.692G>A|p.Gly231Asp |
S125 |
| 76652 | BAA01g40500 | A01 | 26826338 | G | A | missense_variant | MODERATE | c.940G>A|p.Val314Met |
S34 |
| 76653 | BAA01g40500 | A01 | 26826406 | C | T | synonymous_variant | LOW | c.1008C>T|p.Asp336Asp |
S292 |
| 76654 | BAA01g40480 | A01 | 26826985 | C | T | upstream_gene_variant | MODIFIER | c.-3915G>A| |
S240 |
| 76655 | BAA01g40500 | A01 | 26827275 | C | T | missense_variant | MODERATE | c.1474C>T|p.Pro492Ser |
S73 S91 |
| 76656 | BAA01g40500 | A01 | 26827478 | C | T | synonymous_variant | LOW | c.1677C>T|p.Pro559Pro |
S161 |
| 76657 | BAA01g40480 | A01 | 26827692 | G | T | upstream_gene_variant | MODIFIER | c.-4622C>A| |
S184 S196 S198 S199 S2 S201 S228 S248 S26 S260 S288 S305 S32 S38 S46 S62 |
| 76658 | BAA01g40480 | A01 | 26827760 | C | T | upstream_gene_variant | MODIFIER | c.-4690G>A| |
S288 |
| 76659 | BAA01g40510 | A01 | 26829855 | C | T | missense_variant | MODERATE | c.47G>A|p.Gly16Glu |
S7 |
| 76660 | BAA01g40510 | A01 | 26830870 | G | A | upstream_gene_variant | MODIFIER | c.-969C>T| |
S99 |
| 76661 | BAA01g40510 | A01 | 26833598 | T | A | upstream_gene_variant | MODIFIER | c.-3697A>T| |
S138 |
| 76662 | BAA01g40510 | A01 | 26834656 | C | T | upstream_gene_variant | MODIFIER | c.-4755G>A| |
S174 S27 |
| 76663 | BAA01g40520 | A01 | 26835982 | A | T | upstream_gene_variant | MODIFIER | c.-2845T>A| |
S54 |
| 76664 | BAA01g40520 | A01 | 26836205 | G | A | upstream_gene_variant | MODIFIER | c.-3068C>T| |
S138 |
| 76665 | BAA01g40520 | A01 | 26836761 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S264 |
| 76666 | BAA01g40530 | A01 | 26839809 | C | T | upstream_gene_variant | MODIFIER | c.-1957C>T| |
S82 S92 |
| 76667 | BAA01g40530 | A01 | 26842949 | G | A | missense_variant | MODERATE | c.580G>A|p.Asp194Asn |
S126 |
| 76668 | BAA01g40530 | A01 | 26842973 | G | A | missense_variant | MODERATE | c.604G>A|p.Ala202Thr |
S229 |
| 76669 | BAA01g40540 | A01 | 26843134 | G | A | upstream_gene_variant | MODIFIER | c.-4657G>A| |
S159 S188 S243 S276 S298 S299 |
| 76670 | BAA01g40540 | A01 | 26844218 | G | A | upstream_gene_variant | MODIFIER | c.-3573G>A| |
S132 S215 |
| 76671 | BAA01g40540 | A01 | 26844382 | G | A | upstream_gene_variant | MODIFIER | c.-3409G>A| |
S283 |
| 76672 | BAA01g40540 | A01 | 26844408 | G | A | upstream_gene_variant | MODIFIER | c.-3383G>A| |
S245 |
| 76673 | BAA01g40540 | A01 | 26845124 | G | A | upstream_gene_variant | MODIFIER | c.-2667G>A| |
S195 |
| 76674 | BAA01g40540 | A01 | 26845720 | C | T | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S274 |
| 76675 | BAA01g40540 | A01 | 26847436 | C | T | upstream_gene_variant | MODIFIER | c.-355C>T| |
S256 |