| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 161201 | BAA02g08350 | A02 | 3578210 | G | A | splice_region_variant&intron_variant | LOW | c.622-4C>T| |
S105 S106 |
| 161202 | BAA02g08360 | A02 | 3579437 | C | T | missense_variant | MODERATE | c.524G>A|p.Gly175Glu |
S200 |
| 161203 | BAA02g08350 | A02 | 3579574 | C | T | upstream_gene_variant | MODIFIER | c.-305G>A| |
S226 |
| 161204 | BAA02g08360 | A02 | 3579640 | C | T | synonymous_variant | LOW | c.423G>A|p.Gln141Gln |
S211 S227 |
| 161205 | BAA02g08350 | A02 | 3580043 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S209 |
| 161206 | BAA02g08360 | A02 | 3580202 | C | T | missense_variant | MODERATE | c.142G>A|p.Glu48Lys |
S262 |
| 161207 | BAA02g08360 | A02 | 3580289 | C | T | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S99 |
| 161208 | BAA02g08350 | A02 | 3580530 | G | A | upstream_gene_variant | MODIFIER | c.-1261C>T| |
S110 |
| 161209 | BAA02g08350 | A02 | 3581283 | G | A | upstream_gene_variant | MODIFIER | c.-2014C>T| |
S198 |
| 161210 | BAA02g08370 | A02 | 3582708 | C | T | missense_variant | MODERATE | c.715C>T|p.Pro239Ser |
S286 |
| 161211 | BAA02g08350 | A02 | 3583949 | C | T | upstream_gene_variant | MODIFIER | c.-4680G>A| |
S171 |
| 161212 | BAA02g08380 | A02 | 3585519 | C | T | synonymous_variant | LOW | c.693C>T|p.Asp231Asp |
S40 S49 |
| 161213 | BAA02g08390 | A02 | 3586282 | G | A | upstream_gene_variant | MODIFIER | c.-635G>A| |
S156 |
| 161214 | BAA02g08390 | A02 | 3588446 | C | T | missense_variant | MODERATE | c.590C>T|p.Ser197Leu |
S178 |
| 161215 | BAA02g08380 | A02 | 3588623 | G | A | downstream_gene_variant | MODIFIER | c.*2499G>A| |
S232 |
| 161216 | BAA02g08420 | A02 | 3593464 | G | A | upstream_gene_variant | MODIFIER | c.-4242G>A| |
S188 |
| 161217 | BAA02g08420 | A02 | 3594505 | G | A | upstream_gene_variant | MODIFIER | c.-3201G>A| |
S238 |
| 161218 | BAA02g08400 | A02 | 3596417 | G | A | upstream_gene_variant | MODIFIER | c.-398C>T| |
S174 |
| 161219 | BAA02g08410 | A02 | 3596953 | T | G | missense_variant | MODERATE | c.139A>C|p.Asn47His |
S150 |
| 161220 | BAA02g08400 | A02 | 3598076 | C | T | upstream_gene_variant | MODIFIER | c.-2057G>A| |
S138 |
| 161221 | BAA02g08400 | A02 | 3598867 | G | A | upstream_gene_variant | MODIFIER | c.-2848C>T| |
S139 |
| 161222 | BAA02g08400 | A02 | 3598933 | C | T | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S243 |
| 161223 | BAA02g08430 | A02 | 3599339 | C | T | missense_variant | MODERATE | c.20C>T|p.Ser7Leu |
S270 |
| 161224 | BAA02g08430 | A02 | 3599349 | G | A | synonymous_variant | LOW | c.30G>A|p.Ser10Ser |
S126 |
| 161225 | BAA02g08430 | A02 | 3600050 | G | A | missense_variant | MODERATE | c.355G>A|p.Ala119Thr |
S283 |