| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 13901 | BAA01g10850 | A01 | 5003637 | C | T | missense_variant | MODERATE | c.56C>T|p.Ala19Val |
S185 |
| 13902 | BAA01g10860 | A01 | 5003723 | C | T | downstream_gene_variant | MODIFIER | c.*2874G>A| |
S295 S296 |
| 13903 | BAA01g10850 | A01 | 5006054 | G | A | downstream_gene_variant | MODIFIER | c.*78G>A| |
S187 |
| 13904 | BAA01g10860 | A01 | 5010018 | G | A | upstream_gene_variant | MODIFIER | c.-646C>T| |
S10 |
| 13905 | BAA01g10870 | A01 | 5015486 | G | A | synonymous_variant | LOW | c.219C>T|p.Leu73Leu |
S201 |
| 13906 | BAA01g10880 | A01 | 5015574 | G | A | upstream_gene_variant | MODIFIER | c.-510G>A| |
S256 |
| 13907 | BAA01g10870 | A01 | 5015620 | G | A | synonymous_variant | LOW | c.162C>T|p.Val54Val |
S191 |
| 13908 | BAA01g10880 | A01 | 5016103 | G | A | missense_variant | MODERATE | c.20G>A|p.Gly7Glu |
S123 |
| 13909 | BAA01g10870 | A01 | 5016768 | G | A | upstream_gene_variant | MODIFIER | c.-987C>T| |
S13 |
| 13910 | BAA01g10870 | A01 | 5017640 | C | T | upstream_gene_variant | MODIFIER | c.-1859G>A| |
S125 |
| 13911 | BAA01g10880 | A01 | 5018646 | C | T | missense_variant | MODERATE | c.1169C>T|p.Ser390Phe |
S79 S84 |
| 13912 | BAA01g10880 | A01 | 5019184 | C | T | missense_variant | MODERATE | c.1387C>T|p.Leu463Phe |
S16 |
| 13913 | BAA01g10880 | A01 | 5020252 | C | T | synonymous_variant | LOW | c.1887C>T|p.Phe629Phe |
S206 |
| 13914 | BAA01g10880 | A01 | 5020507 | C | T | synonymous_variant | LOW | c.2019C>T|p.Ile673Ile |
S134 |
| 13915 | BAA01g10890 | A01 | 5021172 | C | T | missense_variant | MODERATE | c.961G>A|p.Glu321Lys |
S78 |
| 13916 | BAA01g10890 | A01 | 5021439 | G | A | missense_variant | MODERATE | c.694C>T|p.His232Tyr |
S187 |
| 13917 | BAA01g10890 | A01 | 5021690 | G | A | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S23 |
| 13918 | BAA01g10890 | A01 | 5021746 | C | T | synonymous_variant | LOW | c.387G>A|p.Arg129Arg |
S41 |
| 13919 | BAA01g10890 | A01 | 5022041 | G | A | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S12 |
| 13920 | BAA01g10890 | A01 | 5023358 | G | A | upstream_gene_variant | MODIFIER | c.-1018C>T| |
S287 |
| 13921 | BAA01g10890 | A01 | 5023542 | C | T | upstream_gene_variant | MODIFIER | c.-1202G>A| |
S46 |
| 13922 | BAA01g10890 | A01 | 5023639 | G | A | upstream_gene_variant | MODIFIER | c.-1299C>T| |
S95 |
| 13923 | BAA01g10890 | A01 | 5024385 | G | A | upstream_gene_variant | MODIFIER | c.-2045C>T| |
S84 |
| 13924 | BAA01g10890 | A01 | 5026315 | G | A | upstream_gene_variant | MODIFIER | c.-3975C>T| |
S272 |
| 13925 | BAA01g10890 | A01 | 5026399 | G | A | upstream_gene_variant | MODIFIER | c.-4059C>T| |
S240 |