| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 43551 | BAA01g26660 | A01 | 14968703 | G | A | upstream_gene_variant | MODIFIER | c.-2197C>T| |
S301 S304 |
| 43552 | BAA01g26660 | A01 | 14968742 | C | T | upstream_gene_variant | MODIFIER | c.-2236G>A| |
S151 |
| 43553 | BAA01g26680 | A01 | 14968903 | C | T | missense_variant | MODERATE | c.367G>A|p.Val123Ile |
S176 |
| 43554 | BAA01g26680 | A01 | 14968974 | C | T | missense_variant | MODERATE | c.296G>A|p.Gly99Glu |
S186 |
| 43555 | BAA01g26660 | A01 | 14969114 | G | A | upstream_gene_variant | MODIFIER | c.-2608C>T| |
S37 |
| 43556 | BAA01g26680 | A01 | 14969292 | G | A | missense_variant | MODERATE | c.53C>T|p.Ser18Leu |
S173 |
| 43557 | BAA01g26680 | A01 | 14969311 | G | A | missense_variant | MODERATE | c.34C>T|p.Arg12Trp |
S32 |
| 43558 | BAA01g26660 | A01 | 14969401 | G | A | upstream_gene_variant | MODIFIER | c.-2895C>T| |
S262 |
| 43559 | BAA01g26660 | A01 | 14970562 | C | T | upstream_gene_variant | MODIFIER | c.-4056G>A| |
S183 |
| 43560 | BAA01g26660 | A01 | 14970565 | C | T | upstream_gene_variant | MODIFIER | c.-4059G>A| |
S230 |
| 43561 | BAA01g26660 | A01 | 14971170 | G | A | upstream_gene_variant | MODIFIER | c.-4664C>T| |
S172 S217 |
| 43562 | BAA01g26660 | A01 | 14971182 | C | T | upstream_gene_variant | MODIFIER | c.-4676G>A| |
S235 |
| 43563 | BAA01g26680 | A01 | 14972583 | G | A | upstream_gene_variant | MODIFIER | c.-3239C>T| |
S298 |
| 43564 | BAA01g26690 | A01 | 14974433 | G | A | downstream_gene_variant | MODIFIER | c.*1923C>T| |
S266 |
| 43565 | BAA01g26690 | A01 | 14974773 | C | T | downstream_gene_variant | MODIFIER | c.*1583G>A| |
S64 |
| 43566 | BAA01g26690 | A01 | 14975329 | G | A | downstream_gene_variant | MODIFIER | c.*1027C>T| |
S175 |
| 43567 | BAA01g26690 | A01 | 14976228 | C | T | downstream_gene_variant | MODIFIER | c.*128G>A| |
S249 |
| 43568 | BAA01g26690 | A01 | 14976729 | C | T | missense_variant | MODERATE | c.1376G>A|p.Arg459Lys |
S146 |
| 43569 | BAA01g26690 | A01 | 14976799 | C | T | missense_variant | MODERATE | c.1306G>A|p.Asp436Asn |
S192 |
| 43570 | BAA01g26690 | A01 | 14977084 | G | A | missense_variant | MODERATE | c.1021C>T|p.Pro341Ser |
S92 |
| 43571 | BAA01g26690 | A01 | 14977093 | G | A | missense_variant | MODERATE | c.1012C>T|p.Pro338Ser |
S138 |
| 43572 | BAA01g26690 | A01 | 14977381 | C | T | missense_variant | MODERATE | c.724G>A|p.Asp242Asn |
S232 |
| 43573 | BAA01g26690 | A01 | 14977518 | G | A | missense_variant | MODERATE | c.587C>T|p.Ser196Phe |
S63 |
| 43574 | BAA01g26690 | A01 | 14977798 | C | T | missense_variant | MODERATE | c.307G>A|p.Glu103Lys |
S162 |
| 43575 | BAA01g26690 | A01 | 14977814 | C | T | synonymous_variant | LOW | c.291G>A|p.Leu97Leu |
S128 S162 |