| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 82801 | BAA01g43980 | A01 | 29110799 | C | T | missense_variant | MODERATE | c.841C>T|p.Leu281Phe |
S142 |
| 82802 | BAA01g43990 | A01 | 29113162 | G | A | synonymous_variant | LOW | c.46C>T|p.Leu16Leu |
S218 |
| 82803 | BAA01g43990 | A01 | 29113185 | C | T | missense_variant | MODERATE | c.23G>A|p.Ser8Asn |
S72 S78 |
| 82804 | BAA01g44000 | A01 | 29114527 | G | A | missense_variant | MODERATE | c.10G>A|p.Asp4Asn |
S117 |
| 82805 | BAA01g44000 | A01 | 29114891 | C | T | missense_variant | MODERATE | c.374C>T|p.Ser125Phe |
S4 |
| 82806 | BAA01g44000 | A01 | 29114965 | C | T | missense_variant | MODERATE | c.448C>T|p.Pro150Ser |
S153 S213 |
| 82807 | BAA01g44000 | A01 | 29115406 | G | A | missense_variant&splice_region_variant | MODERATE | c.889G>A|p.Gly297Arg |
S143 |
| 82808 | BAA01g44000 | A01 | 29116200 | G | A | missense_variant | MODERATE | c.1078G>A|p.Asp360Asn |
S98 |
| 82809 | BAA01g43990 | A01 | 29116946 | G | A | upstream_gene_variant | MODIFIER | c.-3739C>T| |
S124 |
| 82810 | BAA01g43990 | A01 | 29117343 | C | T | upstream_gene_variant | MODIFIER | c.-4136G>A| |
S89 |
| 82811 | BAA01g44000 | A01 | 29117477 | G | A | synonymous_variant | LOW | c.1839G>A|p.Lys613Lys |
S1 S90 |
| 82812 | BAA01g44000 | A01 | 29117702 | C | T | missense_variant | MODERATE | c.1979C>T|p.Pro660Leu |
S206 S26 |
| 82813 | BAA01g43990 | A01 | 29117862 | C | T | upstream_gene_variant | MODIFIER | c.-4655G>A| |
S168 |
| 82814 | BAA01g44010 | A01 | 29119303 | C | T | upstream_gene_variant | MODIFIER | c.-800C>T| |
S112 |
| 82815 | BAA01g44010 | A01 | 29119756 | C | T | upstream_gene_variant | MODIFIER | c.-347C>T| |
S39 |
| 82816 | BAA01g44010 | A01 | 29119945 | G | A | upstream_gene_variant | MODIFIER | c.-158G>A| |
S53 |
| 82817 | BAA01g44010 | A01 | 29120270 | C | T | missense_variant | MODERATE | c.79C>T|p.Leu27Phe |
S286 |
| 82818 | BAA01g44010 | A01 | 29120543 | G | A | missense_variant | MODERATE | c.154G>A|p.Gly52Arg |
S169 |
| 82819 | BAA01g44000 | A01 | 29120846 | C | T | downstream_gene_variant | MODIFIER | c.*1811C>T| |
S203 |
| 82820 | BAA01g44020 | A01 | 29121999 | G | A | synonymous_variant | LOW | c.507C>T|p.Thr169Thr |
S298 |
| 82821 | BAA01g44000 | A01 | 29122080 | G | A | downstream_gene_variant | MODIFIER | c.*3045G>A| |
S122 |
| 82822 | BAA01g44000 | A01 | 29122113 | C | T | downstream_gene_variant | MODIFIER | c.*3078C>T| |
S247 |
| 82823 | BAA01g44000 | A01 | 29122159 | G | A | downstream_gene_variant | MODIFIER | c.*3124G>A| |
S123 |
| 82824 | BAA01g44020 | A01 | 29122461 | G | A | missense_variant | MODERATE | c.448C>T|p.Leu150Phe |
S71 |
| 82825 | BAA01g44020 | A01 | 29122722 | G | A | synonymous_variant | LOW | c.187C>T|p.Leu63Leu |
S271 |