| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 68101 | BAA01g35700 | A01 | 23871562 | G | A | missense_variant | MODERATE | c.1274G>A|p.Arg425Lys |
S38 |
| 68102 | BAA01g35690 | A01 | 23872030 | G | A | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S199 |
| 68103 | BAA01g35690 | A01 | 23872474 | G | A | upstream_gene_variant | MODIFIER | c.-2515C>T| |
S74 |
| 68104 | BAA01g35690 | A01 | 23872982 | C | T | upstream_gene_variant | MODIFIER | c.-3023G>A| |
S203 |
| 68105 | BAA01g35690 | A01 | 23873258 | C | T | upstream_gene_variant | MODIFIER | c.-3299G>A| |
S78 S83 |
| 68106 | BAA01g35690 | A01 | 23873489 | C | T | upstream_gene_variant | MODIFIER | c.-3530G>A| |
S301 S304 |
| 68107 | BAA01g35700 | A01 | 23873837 | G | A | synonymous_variant | LOW | c.1683G>A|p.Gly561Gly |
S2 |
| 68108 | BAA01g35700 | A01 | 23873877 | G | A | missense_variant | MODERATE | c.1723G>A|p.Ala575Thr |
S176 |
| 68109 | BAA01g35700 | A01 | 23874233 | C | A | synonymous_variant | LOW | c.2079C>A|p.Thr693Thr |
S87 |
| 68110 | BAA01g35700 | A01 | 23874443 | C | T | synonymous_variant | LOW | c.2289C>T|p.Tyr763Tyr |
S228 |
| 68111 | BAA01g35700 | A01 | 23874457 | C | T | missense_variant | MODERATE | c.2303C>T|p.Ser768Leu |
S117 S295 |
| 68112 | BAA01g35700 | A01 | 23874531 | C | T | missense_variant | MODERATE | c.2377C>T|p.Pro793Ser |
S4 |
| 68113 | BAA01g35700 | A01 | 23874981 | C | T | missense_variant | MODERATE | c.2827C>T|p.Pro943Ser |
S238 |
| 68114 | BAA01g35700 | A01 | 23875629 | C | T | downstream_gene_variant | MODIFIER | c.*559C>T| |
S46 |
| 68115 | BAA01g35700 | A01 | 23876552 | C | T | downstream_gene_variant | MODIFIER | c.*1482C>T| |
S238 |
| 68116 | BAA01g35700 | A01 | 23876866 | G | A | downstream_gene_variant | MODIFIER | c.*1796G>A| |
S70 |
| 68117 | BAA01g35700 | A01 | 23877193 | G | A | downstream_gene_variant | MODIFIER | c.*2123G>A| |
S87 |
| 68118 | BAA01g35700 | A01 | 23877196 | G | A | downstream_gene_variant | MODIFIER | c.*2126G>A| |
S121 |
| 68119 | BAA01g35710 | A01 | 23877789 | G | A | missense_variant | MODERATE | c.3118C>T|p.Leu1040Phe |
S104 S52 |
| 68120 | BAA01g35710 | A01 | 23878210 | C | T | synonymous_variant | LOW | c.2697G>A|p.Leu899Leu |
S75 S81 |
| 68121 | BAA01g35710 | A01 | 23878403 | G | A | missense_variant | MODERATE | c.2504C>T|p.Thr835Ile |
S38 |
| 68122 | BAA01g35710 | A01 | 23878427 | G | A | missense_variant | MODERATE | c.2480C>T|p.Ala827Val |
S297 |
| 68123 | BAA01g35700 | A01 | 23879179 | G | A | downstream_gene_variant | MODIFIER | c.*4109G>A| |
S227 |
| 68124 | BAA01g35700 | A01 | 23879242 | G | A | downstream_gene_variant | MODIFIER | c.*4172G>A| |
S241 |
| 68125 | BAA01g35710 | A01 | 23879856 | G | A | missense_variant | MODERATE | c.1283C>T|p.Thr428Ile |
S72 S78 |