| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 25801 | BAA01g18480 | A01 | 9059161 | G | A | missense_variant | MODERATE | c.611G>A|p.Ser204Asn |
S162 |
| 25802 | BAA01g18480 | A01 | 9059841 | G | A | missense_variant | MODERATE | c.817G>A|p.Asp273Asn |
S159 S243 |
| 25803 | BAA01g18480 | A01 | 9059898 | G | A | missense_variant | MODERATE | c.874G>A|p.Glu292Lys |
S308 |
| 25804 | BAA01g18480 | A01 | 9060131 | G | A | synonymous_variant | LOW | c.1107G>A|p.Leu369Leu |
S23 |
| 25805 | BAA01g18480 | A01 | 9060376 | C | T | missense_variant | MODERATE | c.1256C>T|p.Pro419Leu |
S294 |
| 25806 | BAA01g18480 | A01 | 9060448 | C | T | missense_variant | MODERATE | c.1328C>T|p.Ala443Val |
S296 |
| 25807 | BAA01g18470 | A01 | 9060621 | C | T | upstream_gene_variant | MODIFIER | c.-2919G>A| |
S295 |
| 25808 | BAA01g18480 | A01 | 9063467 | G | A | downstream_gene_variant | MODIFIER | c.*1452G>A| |
S202 |
| 25809 | BAA01g18490 | A01 | 9064874 | C | T | synonymous_variant | LOW | c.1476G>A|p.Gly492Gly |
S260 |
| 25810 | BAA01g18490 | A01 | 9065055 | C | T | missense_variant | MODERATE | c.1295G>A|p.Arg432Gln |
S242 |
| 25811 | BAA01g18490 | A01 | 9065139 | C | T | missense_variant | MODERATE | c.1211G>A|p.Arg404Gln |
S117 |
| 25812 | BAA01g18490 | A01 | 9065141 | C | T | stop_gained | HIGH | c.1209G>A|p.Trp403* |
S264 |
| 25813 | BAA01g18490 | A01 | 9065190 | G | A | missense_variant | MODERATE | c.1160C>T|p.Ser387Leu |
S15 S156 S2 S213 S3 S4 S6 |
| 25814 | BAA01g18490 | A01 | 9065279 | C | T | synonymous_variant | LOW | c.1071G>A|p.Val357Val |
S176 |
| 25815 | BAA01g18490 | A01 | 9065302 | C | T | missense_variant | MODERATE | c.1048G>A|p.Gly350Arg |
S16 |
| 25816 | BAA01g18480 | A01 | 9065652 | G | A | downstream_gene_variant | MODIFIER | c.*3637G>A| |
S129 |
| 25817 | BAA01g18490 | A01 | 9065723 | G | A | synonymous_variant | LOW | c.840C>T|p.Asn280Asn |
S196 |
| 25818 | BAA01g18490 | A01 | 9065755 | C | T | missense_variant | MODERATE | c.808G>A|p.Glu270Lys |
S67 |
| 25819 | BAA01g18490 | A01 | 9065894 | G | A | synonymous_variant | LOW | c.669C>T|p.Ile223Ile |
S249 |
| 25820 | BAA01g18490 | A01 | 9065899 | C | T | missense_variant | MODERATE | c.664G>A|p.Glu222Lys |
S133 |
| 25821 | BAA01g18490 | A01 | 9065953 | G | A | synonymous_variant | LOW | c.610C>T|p.Leu204Leu |
S139 |
| 25822 | BAA01g18480 | A01 | 9066510 | C | T | downstream_gene_variant | MODIFIER | c.*4495C>T| |
S70 |
| 25823 | BAA01g18480 | A01 | 9066606 | C | T | downstream_gene_variant | MODIFIER | c.*4591C>T| |
S128 |
| 25824 | BAA01g18480 | A01 | 9066694 | C | T | downstream_gene_variant | MODIFIER | c.*4679C>T| |
S216 |
| 25825 | BAA01g18490 | A01 | 9066993 | G | A | synonymous_variant | LOW | c.28C>T|p.Leu10Leu |
S201 |