| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154201 | BAA02g02540 | A02 | 1145386 | G | A | upstream_gene_variant | MODIFIER | c.-839G>A| |
S223 |
| 154202 | BAA02g02540 | A02 | 1146098 | G | A | upstream_gene_variant | MODIFIER | c.-127G>A| |
S134 |
| 154203 | BAA02g02540 | A02 | 1146443 | G | A | synonymous_variant | LOW | c.219G>A|p.Leu73Leu |
S25 |
| 154204 | BAA02g02540 | A02 | 1147588 | G | A | missense_variant | MODERATE | c.589G>A|p.Asp197Asn |
S302 |
| 154205 | BAA02g02540 | A02 | 1149326 | G | A | downstream_gene_variant | MODIFIER | c.*1703G>A| |
S180 S48 |
| 154206 | BAA02g02540 | A02 | 1151203 | G | A | downstream_gene_variant | MODIFIER | c.*3580G>A| |
S125 |
| 154207 | BAA02g02540 | A02 | 1151957 | G | A | downstream_gene_variant | MODIFIER | c.*4334G>A| |
S60 |
| 154208 | BAA02g02550 | A02 | 1152649 | C | T | downstream_gene_variant | MODIFIER | c.*1619G>A| |
S142 |
| 154209 | BAA02g02550 | A02 | 1153130 | C | T | downstream_gene_variant | MODIFIER | c.*1138G>A| |
S200 |
| 154210 | BAA02g02550 | A02 | 1153451 | C | T | downstream_gene_variant | MODIFIER | c.*817G>A| |
S61 |
| 154211 | BAA02g02550 | A02 | 1154812 | G | A | missense_variant | MODERATE | c.5915C>T|p.Ser1972Phe |
S293 |
| 154212 | BAA02g02550 | A02 | 1156228 | C | T | missense_variant | MODERATE | c.4499G>A|p.Gly1500Glu |
S159 |
| 154213 | BAA02g02550 | A02 | 1157125 | C | T | missense_variant | MODERATE | c.3602G>A|p.Gly1201Glu |
S277 |
| 154214 | BAA02g02550 | A02 | 1157506 | C | T | missense_variant | MODERATE | c.3221G>A|p.Ser1074Asn |
S94 |
| 154215 | BAA02g02550 | A02 | 1158022 | C | T | missense_variant | MODERATE | c.2705G>A|p.Gly902Glu |
S240 |
| 154216 | BAA02g02550 | A02 | 1158370 | C | T | missense_variant | MODERATE | c.2357G>A|p.Gly786Glu |
S234 |
| 154217 | BAA02g02550 | A02 | 1158547 | G | A | missense_variant | MODERATE | c.2180C>T|p.Ser727Leu |
S165 |
| 154218 | BAA02g02550 | A02 | 1159368 | G | A | synonymous_variant | LOW | c.1359C>T|p.Pro453Pro |
S107 |
| 154219 | BAA02g02550 | A02 | 1159603 | C | T | missense_variant | MODERATE | c.1124G>A|p.Ser375Asn |
S88 |
| 154220 | BAA02g02550 | A02 | 1159730 | C | T | missense_variant | MODERATE | c.997G>A|p.Gly333Ser |
S15 S3 |
| 154221 | BAA02g02550 | A02 | 1160145 | C | T | synonymous_variant | LOW | c.582G>A|p.Leu194Leu |
S61 |
| 154222 | BAA02g02560 | A02 | 1161006 | G | A | upstream_gene_variant | MODIFIER | c.-3030G>A| |
S81 S85 |
| 154223 | BAA02g02550 | A02 | 1161995 | G | A | upstream_gene_variant | MODIFIER | c.-388C>T| |
S107 |
| 154224 | BAA02g02560 | A02 | 1164248 | G | A | synonymous_variant | LOW | c.213G>A|p.Leu71Leu |
S206 S26 |
| 154225 | BAA02g02570 | A02 | 1167461 | G | A | synonymous_variant | LOW | c.99C>T|p.Leu33Leu |
S166 |