| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 169351 | BAA02g14480 | A02 | 6770921 | C | T | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S182 |
| 169352 | BAA02g14480 | A02 | 6771848 | C | T | upstream_gene_variant | MODIFIER | c.-275C>T| |
S255 |
| 169353 | BAA02g14480 | A02 | 6773601 | G | A | missense_variant | MODERATE | c.1045G>A|p.Gly349Arg |
S36 |
| 169354 | BAA02g14470 | A02 | 6774291 | C | T | downstream_gene_variant | MODIFIER | c.*4261C>T| |
S262 |
| 169355 | BAA02g14470 | A02 | 6774305 | A | T | downstream_gene_variant | MODIFIER | c.*4275A>T| |
S44 |
| 169356 | BAA02g14470 | A02 | 6774351 | C | T | downstream_gene_variant | MODIFIER | c.*4321C>T| |
S44 |
| 169357 | BAA02g14470 | A02 | 6774649 | G | A | downstream_gene_variant | MODIFIER | c.*4619G>A| |
S136 |
| 169358 | BAA02g14490 | A02 | 6775023 | G | A | stop_gained | HIGH | c.1615C>T|p.Gln539* |
S187 |
| 169359 | BAA02g14490 | A02 | 6775214 | C | T | missense_variant | MODERATE | c.1424G>A|p.Arg475Lys |
S142 |
| 169360 | BAA02g14490 | A02 | 6776688 | C | T | missense_variant | MODERATE | c.1138G>A|p.Val380Ile |
S88 |
| 169361 | BAA02g14490 | A02 | 6777078 | G | A | stop_gained | HIGH | c.748C>T|p.Arg250* |
S105 S106 |
| 169362 | BAA02g14490 | A02 | 6777105 | G | A | missense_variant | MODERATE | c.721C>T|p.Leu241Phe |
S162 |
| 169363 | BAA02g14490 | A02 | 6777446 | G | A | missense_variant | MODERATE | c.380C>T|p.Ser127Phe |
S157 |
| 169364 | BAA02g14490 | A02 | 6778416 | C | T | upstream_gene_variant | MODIFIER | c.-423G>A| |
S249 |
| 169365 | BAA02g14490 | A02 | 6778505 | C | T | upstream_gene_variant | MODIFIER | c.-512G>A| |
S63 |
| 169366 | BAA02g14490 | A02 | 6778520 | G | A | upstream_gene_variant | MODIFIER | c.-527C>T| |
S125 |
| 169367 | BAA02g14490 | A02 | 6779563 | C | T | upstream_gene_variant | MODIFIER | c.-1570G>A| |
S216 S241 S265 S39 |
| 169368 | BAA02g14490 | A02 | 6780115 | C | T | upstream_gene_variant | MODIFIER | c.-2122G>A| |
S179 |
| 169369 | BAA02g14500 | A02 | 6780744 | C | T | splice_region_variant&intron_variant | LOW | c.1320+5G>A| |
S79 S84 |
| 169370 | BAA02g14500 | A02 | 6782147 | G | A | missense_variant | MODERATE | c.409C>T|p.Pro137Ser |
S166 |
| 169371 | BAA02g14500 | A02 | 6782507 | G | A | stop_gained | HIGH | c.214C>T|p.Arg72* |
S265 |
| 169372 | BAA02g14500 | A02 | 6782518 | C | T | missense_variant | MODERATE | c.203G>A|p.Gly68Glu |
S230 S85 |
| 169373 | BAA02g14500 | A02 | 6784563 | C | T | upstream_gene_variant | MODIFIER | c.-1843G>A| |
S212 |
| 169374 | BAA02g14510 | A02 | 6787053 | G | A | synonymous_variant | LOW | c.405G>A|p.Lys135Lys |
S136 |
| 169375 | BAA02g14500 | A02 | 6787652 | C | T | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S40 S49 |