| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167601 | BAA02g13260 | A02 | 6025024 | G | A | missense_variant | MODERATE | c.763G>A|p.Ala255Thr |
S247 |
| 167602 | BAA02g13260 | A02 | 6025375 | G | A | missense_variant | MODERATE | c.1114G>A|p.Glu372Lys |
S162 |
| 167603 | BAA02g13260 | A02 | 6025464 | C | T | synonymous_variant | LOW | c.1203C>T|p.Phe401Phe |
S278 |
| 167604 | BAA02g13260 | A02 | 6025485 | G | A | synonymous_variant | LOW | c.1224G>A|p.Lys408Lys |
S119 |
| 167605 | BAA02g13260 | A02 | 6026049 | G | A | missense_variant | MODERATE | c.1636G>A|p.Asp546Asn |
S303 |
| 167606 | BAA02g13260 | A02 | 6026385 | G | A | missense_variant | MODERATE | c.1886G>A|p.Ser629Asn |
S2 |
| 167607 | BAA02g13260 | A02 | 6027350 | C | T | synonymous_variant | LOW | c.2520C>T|p.Leu840Leu |
S282 |
| 167608 | BAA02g13260 | A02 | 6029223 | G | A | downstream_gene_variant | MODIFIER | c.*1337G>A| |
S295 |
| 167609 | BAA02g13260 | A02 | 6029691 | G | A | downstream_gene_variant | MODIFIER | c.*1805G>A| |
S113 |
| 167610 | BAA02g13280 | A02 | 6030218 | C | T | synonymous_variant | LOW | c.642G>A|p.Lys214Lys |
S58 |
| 167611 | BAA02g13280 | A02 | 6031350 | G | A | upstream_gene_variant | MODIFIER | c.-35C>T| |
S302 |
| 167612 | BAA02g13280 | A02 | 6031536 | C | T | upstream_gene_variant | MODIFIER | c.-221G>A| |
S32 |
| 167613 | BAA02g13280 | A02 | 6032645 | G | A | upstream_gene_variant | MODIFIER | c.-1330C>T| |
S87 |
| 167614 | BAA02g13280 | A02 | 6035541 | G | A | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S159 S243 |
| 167615 | BAA02g13280 | A02 | 6036287 | G | A | upstream_gene_variant | MODIFIER | c.-4972C>T| |
S132 S137 S215 S89 |
| 167616 | BAA02g13290 | A02 | 6037068 | G | A | upstream_gene_variant | MODIFIER | c.-3247G>A| |
S260 |
| 167617 | BAA02g13290 | A02 | 6040368 | G | A | synonymous_variant | LOW | c.54G>A|p.Gln18Gln |
S159 S243 |
| 167618 | BAA02g13290 | A02 | 6042679 | G | A | missense_variant | MODERATE | c.1132G>A|p.Ala378Thr |
S275 |
| 167619 | BAA02g13290 | A02 | 6043381 | G | A | downstream_gene_variant | MODIFIER | c.*649G>A| |
S202 |
| 167620 | BAA02g13290 | A02 | 6046898 | C | T | downstream_gene_variant | MODIFIER | c.*4166C>T| |
S293 |
| 167621 | BAA02g13300 | A02 | 6047992 | C | T | downstream_gene_variant | MODIFIER | c.*690G>A| |
S283 |
| 167622 | BAA02g13300 | A02 | 6048047 | G | A | downstream_gene_variant | MODIFIER | c.*635C>T| |
S225 |
| 167623 | BAA02g13300 | A02 | 6049229 | G | A | synonymous_variant | LOW | c.3450C>T|p.Val1150Val |
S34 |
| 167624 | BAA02g13300 | A02 | 6049287 | G | A | missense_variant | MODERATE | c.3392C>T|p.Thr1131Ile |
S92 |
| 167625 | BAA02g13300 | A02 | 6049440 | G | A | intron_variant | MODIFIER | c.3320+9C>T| |
S192 |