| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154401 | BAA02g02650 | A02 | 1210074 | C | T | upstream_gene_variant | MODIFIER | c.-1116G>A| |
S56 |
| 154402 | BAA02g02650 | A02 | 1211582 | C | T | upstream_gene_variant | MODIFIER | c.-2624G>A| |
S153 |
| 154403 | BAA02g02650 | A02 | 1212992 | C | T | upstream_gene_variant | MODIFIER | c.-4034G>A| |
S61 |
| 154404 | BAA02g02660 | A02 | 1214732 | C | T | synonymous_variant | LOW | c.855C>T|p.Ser285Ser |
S185 |
| 154405 | BAA02g02660 | A02 | 1214921 | G | A | stop_gained | HIGH | c.1044G>A|p.Trp348* |
S170 |
| 154406 | BAA02g02670 | A02 | 1215586 | C | T | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S171 |
| 154407 | BAA02g02670 | A02 | 1216870 | C | T | missense_variant | MODERATE | c.1361C>T|p.Ser454Phe |
S160 |
| 154408 | BAA02g02680 | A02 | 1220117 | G | A | upstream_gene_variant | MODIFIER | c.-911C>T| |
S246 |
| 154409 | BAA02g02680 | A02 | 1220795 | G | A | upstream_gene_variant | MODIFIER | c.-1589C>T| |
S155 S211 |
| 154410 | BAA02g02690 | A02 | 1221730 | G | A | synonymous_variant | LOW | c.2161C>T|p.Leu721Leu |
S176 |
| 154411 | BAA02g02690 | A02 | 1221847 | C | T | missense_variant | MODERATE | c.2044G>A|p.Ala682Thr |
S81 S85 |
| 154412 | BAA02g02690 | A02 | 1221871 | G | A | splice_region_variant&intron_variant | LOW | c.2026-6C>T| |
S158 |
| 154413 | BAA02g02680 | A02 | 1222941 | G | A | upstream_gene_variant | MODIFIER | c.-3735C>T| |
S273 |
| 154414 | BAA02g02680 | A02 | 1223011 | C | T | upstream_gene_variant | MODIFIER | c.-3805G>A| |
S39 |
| 154415 | BAA02g02690 | A02 | 1223284 | C | T | missense_variant | MODERATE | c.1282G>A|p.Asp428Asn |
S281 |
| 154416 | BAA02g02690 | A02 | 1223319 | C | T | missense_variant | MODERATE | c.1247G>A|p.Gly416Glu |
S117 |
| 154417 | BAA02g02690 | A02 | 1223391 | G | A | missense_variant | MODERATE | c.1175C>T|p.Ser392Leu |
S158 |
| 154418 | BAA02g02690 | A02 | 1223801 | G | A | missense_variant | MODERATE | c.862C>T|p.Pro288Ser |
S67 |
| 154419 | BAA02g02690 | A02 | 1223810 | C | T | missense_variant | MODERATE | c.853G>A|p.Asp285Asn |
S250 |
| 154420 | BAA02g02690 | A02 | 1223822 | C | T | missense_variant | MODERATE | c.841G>A|p.Glu281Lys |
S15 S3 |
| 154421 | BAA02g02690 | A02 | 1224393 | G | A | synonymous_variant | LOW | c.270C>T|p.Cys90Cys |
S271 |
| 154422 | BAA02g02690 | A02 | 1225119 | C | T | upstream_gene_variant | MODIFIER | c.-457G>A| |
S16 |
| 154423 | BAA02g02690 | A02 | 1225680 | C | T | upstream_gene_variant | MODIFIER | c.-1018G>A| |
S119 |
| 154424 | BAA02g02690 | A02 | 1226097 | G | A | upstream_gene_variant | MODIFIER | c.-1435C>T| |
S236 |
| 154425 | BAA02g02690 | A02 | 1227350 | C | T | upstream_gene_variant | MODIFIER | c.-2688G>A| |
S228 S250 |