| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155551 | BAA02g03650 | A02 | 1612406 | C | T | missense_variant | MODERATE | c.836G>A|p.Arg279Lys |
S75 |
| 155552 | BAA02g03650 | A02 | 1612821 | G | A | synonymous_variant | LOW | c.708C>T|p.Leu236Leu |
S302 |
| 155553 | BAA02g03650 | A02 | 1613607 | G | A | splice_region_variant&synonymous_variant | LOW | c.432C>T|p.Phe144Phe |
S209 |
| 155554 | BAA02g03650 | A02 | 1613739 | C | T | synonymous_variant | LOW | c.300G>A|p.Lys100Lys |
S34 |
| 155555 | BAA02g03650 | A02 | 1613869 | C | T | missense_variant | MODERATE | c.245G>A|p.Gly82Glu |
S202 |
| 155556 | BAA02g03650 | A02 | 1614661 | C | T | upstream_gene_variant | MODIFIER | c.-403G>A| |
S243 S299 |
| 155557 | BAA02g03650 | A02 | 1615337 | G | A | upstream_gene_variant | MODIFIER | c.-1079C>T| |
S122 |
| 155558 | BAA02g03650 | A02 | 1616308 | G | A | upstream_gene_variant | MODIFIER | c.-2050C>T| |
S202 |
| 155559 | BAA02g03650 | A02 | 1617350 | G | A | upstream_gene_variant | MODIFIER | c.-3092C>T| |
S12 |
| 155560 | BAA02g03660 | A02 | 1617587 | C | T | synonymous_variant | LOW | c.129G>A|p.Ala43Ala |
S138 |
| 155561 | BAA02g03650 | A02 | 1617661 | G | A | upstream_gene_variant | MODIFIER | c.-3403C>T| |
S23 |
| 155562 | BAA02g03650 | A02 | 1618224 | G | A | upstream_gene_variant | MODIFIER | c.-3966C>T| |
S28 |
| 155563 | BAA02g03650 | A02 | 1618343 | G | A | upstream_gene_variant | MODIFIER | c.-4085C>T| |
S17 |
| 155564 | BAA02g03650 | A02 | 1618535 | G | A | upstream_gene_variant | MODIFIER | c.-4277C>T| |
S23 |
| 155565 | BAA02g03670 | A02 | 1619366 | C | T | missense_variant | MODERATE | c.713G>A|p.Arg238Lys |
S15 S2 S3 S34 |
| 155566 | BAA02g03670 | A02 | 1619482 | C | T | synonymous_variant | LOW | c.597G>A|p.Lys199Lys |
S280 |
| 155567 | BAA02g03670 | A02 | 1619523 | G | A | missense_variant | MODERATE | c.556C>T|p.Pro186Ser |
S293 |
| 155568 | BAA02g03670 | A02 | 1620036 | C | A | missense_variant | MODERATE | c.118G>T|p.Ala40Ser |
S270 |
| 155569 | BAA02g03680 | A02 | 1621550 | C | T | missense_variant | MODERATE | c.41G>A|p.Gly14Asp |
S32 |
| 155570 | BAA02g03690 | A02 | 1622814 | C | T | missense_variant | MODERATE | c.1319G>A|p.Gly440Asp |
S172 |
| 155571 | BAA02g03670 | A02 | 1623326 | G | A | upstream_gene_variant | MODIFIER | c.-2903C>T| |
S205 |
| 155572 | BAA02g03680 | A02 | 1625529 | G | A | upstream_gene_variant | MODIFIER | c.-3939C>T| |
S261 |
| 155573 | BAA02g03690 | A02 | 1627276 | C | T | upstream_gene_variant | MODIFIER | c.-2610G>A| |
S252 |
| 155574 | BAA02g03690 | A02 | 1628653 | G | A | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S168 |
| 155575 | BAA02g03700 | A02 | 1628998 | C | T | missense_variant&splice_region_variant | MODERATE | c.692G>A|p.Gly231Asp |
S104 |