| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 25751 | BAA01g18440 | A01 | 9050051 | C | T | upstream_gene_variant | MODIFIER | c.-4348G>A| |
S184 |
| 25752 | BAA01g18440 | A01 | 9050457 | G | A | upstream_gene_variant | MODIFIER | c.-4754C>T| |
S131 |
| 25753 | BAA01g18460 | A01 | 9051212 | G | A | missense_variant&splice_region_variant | MODERATE | c.283G>A|p.Glu95Lys |
S275 |
| 25754 | BAA01g18460 | A01 | 9051991 | C | T | missense_variant | MODERATE | c.1000C>T|p.Leu334Phe |
S61 |
| 25755 | BAA01g18460 | A01 | 9052034 | C | T | missense_variant | MODERATE | c.1043C>T|p.Ser348Phe |
S46 |
| 25756 | BAA01g18450 | A01 | 9052095 | G | A | downstream_gene_variant | MODIFIER | c.*2055G>A| |
S139 |
| 25757 | BAA01g18450 | A01 | 9052261 | C | T | downstream_gene_variant | MODIFIER | c.*2221C>T| |
S2 |
| 25758 | BAA01g18480 | A01 | 9053441 | C | T | upstream_gene_variant | MODIFIER | c.-4933C>T| |
S250 |
| 25759 | BAA01g18480 | A01 | 9054187 | G | A | upstream_gene_variant | MODIFIER | c.-4187G>A| |
S168 |
| 25760 | BAA01g18470 | A01 | 9055601 | G | A | missense_variant | MODERATE | c.2102C>T|p.Ser701Phe |
S86 |
| 25761 | BAA01g18470 | A01 | 9055643 | G | A | missense_variant | MODERATE | c.2060C>T|p.Ser687Phe |
S169 |
| 25762 | BAA01g18470 | A01 | 9055983 | G | A | synonymous_variant | LOW | c.1720C>T|p.Leu574Leu |
S58 |
| 25763 | BAA01g18470 | A01 | 9056044 | G | A | synonymous_variant | LOW | c.1659C>T|p.Leu553Leu |
S287 |
| 25764 | BAA01g18470 | A01 | 9056158 | G | A | synonymous_variant | LOW | c.1545C>T|p.Ser515Ser |
S34 |
| 25765 | BAA01g18470 | A01 | 9056207 | G | A | missense_variant | MODERATE | c.1496C>T|p.Ser499Phe |
S138 |
| 25766 | BAA01g18470 | A01 | 9056239 | G | A | synonymous_variant | LOW | c.1464C>T|p.Asn488Asn |
S252 |
| 25767 | BAA01g18470 | A01 | 9056958 | G | A | synonymous_variant | LOW | c.745C>T|p.Leu249Leu |
S131 |
| 25768 | BAA01g18470 | A01 | 9056965 | G | A | synonymous_variant | LOW | c.738C>T|p.Tyr246Tyr |
S168 |
| 25769 | BAA01g18470 | A01 | 9056982 | G | A | stop_gained | HIGH | c.721C>T|p.Gln241* |
S86 |
| 25770 | BAA01g18470 | A01 | 9057144 | C | T | missense_variant | MODERATE | c.559G>A|p.Glu187Lys |
S305 |
| 25771 | BAA01g18470 | A01 | 9057722 | G | A | upstream_gene_variant | MODIFIER | c.-20C>T| |
S212 |
| 25772 | BAA01g18470 | A01 | 9057775 | G | A | upstream_gene_variant | MODIFIER | c.-73C>T| |
S84 S93 |
| 25773 | BAA01g18480 | A01 | 9058522 | C | T | missense_variant | MODERATE | c.149C>T|p.Thr50Met |
S230 |
| 25774 | BAA01g18480 | A01 | 9058960 | C | T | missense_variant | MODERATE | c.410C>T|p.Ala137Val |
S82 S92 |
| 25775 | BAA01g18480 | A01 | 9059145 | G | A | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S237 |