| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 21001 | BAA01g15390 | A01 | 7402950 | G | A | missense_variant | MODERATE | c.1154C>T|p.Ala385Val |
S59 |
| 21002 | BAA01g15390 | A01 | 7404311 | C | T | synonymous_variant | LOW | c.126G>A|p.Gly42Gly |
S296 |
| 21003 | BAA01g15390 | A01 | 7404638 | G | A | upstream_gene_variant | MODIFIER | c.-202C>T| |
S190 |
| 21004 | BAA01g15390 | A01 | 7405304 | G | A | upstream_gene_variant | MODIFIER | c.-868C>T| |
S13 |
| 21005 | BAA01g15390 | A01 | 7405797 | C | T | upstream_gene_variant | MODIFIER | c.-1361G>A| |
S192 |
| 21006 | BAA01g15390 | A01 | 7406503 | G | A | upstream_gene_variant | MODIFIER | c.-2067C>T| |
S281 |
| 21007 | BAA01g15390 | A01 | 7408831 | G | A | upstream_gene_variant | MODIFIER | c.-4395C>T| |
S115 |
| 21008 | BAA01g15390-BAA01g15400 | A01 | 7409510 | C | T | intergenic_region | MODIFIER | n.7409510C>T| |
S234 |
| 21009 | BAA01g15390-BAA01g15400 | A01 | 7410081 | C | T | intergenic_region | MODIFIER | n.7410081C>T| |
S99 |
| 21010 | BAA01g15390-BAA01g15400 | A01 | 7417016 | C | T | intergenic_region | MODIFIER | n.7417016C>T| |
S289 S290 |
| 21011 | BAA01g15390-BAA01g15400 | A01 | 7417407 | C | T | intergenic_region | MODIFIER | n.7417407C>T| |
S167 |
| 21012 | BAA01g15400 | A01 | 7418179 | C | T | upstream_gene_variant | MODIFIER | c.-4317C>T| |
S128 |
| 21013 | BAA01g15400 | A01 | 7419420 | C | T | upstream_gene_variant | MODIFIER | c.-3076C>T| |
S138 |
| 21014 | BAA01g15400 | A01 | 7419663 | C | T | upstream_gene_variant | MODIFIER | c.-2833C>T| |
S179 |
| 21015 | BAA01g15400 | A01 | 7421065 | C | T | upstream_gene_variant | MODIFIER | c.-1431C>T| |
S118 |
| 21016 | BAA01g15400 | A01 | 7422319 | C | T | upstream_gene_variant | MODIFIER | c.-177C>T| |
S4 |
| 21017 | BAA01g15400 | A01 | 7422338 | A | C | upstream_gene_variant | MODIFIER | c.-158A>C| |
S4 |
| 21018 | BAA01g15400 | A01 | 7422727 | G | A | missense_variant | MODERATE | c.232G>A|p.Asp78Asn |
S187 |
| 21019 | BAA01g15410 | A01 | 7423241 | C | T | downstream_gene_variant | MODIFIER | c.*4263G>A| |
S148 S30 S31 |
| 21020 | BAA01g15400 | A01 | 7423590 | G | A | missense_variant | MODERATE | c.658G>A|p.Val220Met |
S59 |
| 21021 | BAA01g15400 | A01 | 7423696 | G | A | missense_variant | MODERATE | c.764G>A|p.Gly255Glu |
S116 |
| 21022 | BAA01g15400 | A01 | 7424828 | C | T | downstream_gene_variant | MODIFIER | c.*1005C>T| |
S198 |
| 21023 | BAA01g15400 | A01 | 7425631 | G | A | downstream_gene_variant | MODIFIER | c.*1808G>A| |
S183 |
| 21024 | BAA01g15400 | A01 | 7427361 | C | T | downstream_gene_variant | MODIFIER | c.*3538C>T| |
S184 |
| 21025 | BAA01g15400 | A01 | 7427415 | C | T | downstream_gene_variant | MODIFIER | c.*3592C>T| |
S295 |