| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 171351 | BAA02g15590 | A02 | 7531126 | C | T | upstream_gene_variant | MODIFIER | c.-2072C>T| |
S283 |
| 171352 | BAA02g15590 | A02 | 7533196 | G | A | upstream_gene_variant | MODIFIER | c.-2G>A| |
S229 |
| 171353 | BAA02g15600 | A02 | 7534550 | G | A | upstream_gene_variant | MODIFIER | c.-3950G>A| |
S51 |
| 171354 | BAA02g15600 | A02 | 7535629 | G | C | upstream_gene_variant | MODIFIER | c.-2871G>C| |
S125 |
| 171355 | BAA02g15600 | A02 | 7535765 | G | A | upstream_gene_variant | MODIFIER | c.-2735G>A| |
S207 |
| 171356 | BAA02g15600 | A02 | 7537906 | C | T | upstream_gene_variant | MODIFIER | c.-594C>T| |
S23 |
| 171357 | BAA02g15600 | A02 | 7538161 | C | T | upstream_gene_variant | MODIFIER | c.-339C>T| |
S181 |
| 171358 | BAA02g15600 | A02 | 7538362 | C | T | upstream_gene_variant | MODIFIER | c.-138C>T| |
S186 |
| 171359 | BAA02g15600 | A02 | 7539175 | G | A | missense_variant | MODERATE | c.676G>A|p.Glu226Lys |
S264 |
| 171360 | BAA02g15600 | A02 | 7539405 | C | T | synonymous_variant | LOW | c.906C>T|p.Val302Val |
S63 |
| 171361 | BAA02g15600 | A02 | 7539427 | G | A | missense_variant | MODERATE | c.928G>A|p.Asp310Asn |
S187 |
| 171362 | BAA02g15600 | A02 | 7539680 | C | T | missense_variant | MODERATE | c.1028C>T|p.Thr343Met |
S25 |
| 171363 | BAA02g15600 | A02 | 7540818 | C | T | downstream_gene_variant | MODIFIER | c.*95C>T| |
S182 |
| 171364 | BAA02g15600 | A02 | 7541509 | C | T | downstream_gene_variant | MODIFIER | c.*786C>T| |
S216 S241 S265 S39 |
| 171365 | BAA02g15600 | A02 | 7542235 | G | A | downstream_gene_variant | MODIFIER | c.*1512G>A| |
S37 |
| 171366 | BAA02g15600 | A02 | 7542375 | G | A | downstream_gene_variant | MODIFIER | c.*1652G>A| |
S62 |
| 171367 | BAA02g15610 | A02 | 7542909 | G | A | synonymous_variant | LOW | c.192C>T|p.Asp64Asp |
S231 |
| 171368 | BAA02g15610 | A02 | 7542919 | G | A | missense_variant | MODERATE | c.182C>T|p.Ser61Leu |
S146 |
| 171369 | BAA02g15610 | A02 | 7543115 | C | T | missense_variant | MODERATE | c.91G>A|p.Gly31Ser |
S38 |
| 171370 | BAA02g15610 | A02 | 7543484 | C | A | splice_region_variant&intron_variant | LOW | c.67+7G>T| |
S84 S93 |
| 171371 | BAA02g15610 | A02 | 7543683 | G | A | upstream_gene_variant | MODIFIER | c.-126C>T| |
S187 |
| 171372 | BAA02g15610 | A02 | 7543710 | C | T | upstream_gene_variant | MODIFIER | c.-153G>A| |
S178 |
| 171373 | BAA02g15610 | A02 | 7543802 | C | T | upstream_gene_variant | MODIFIER | c.-245G>A| |
S138 |
| 171374 | BAA02g15610 | A02 | 7545086 | C | T | upstream_gene_variant | MODIFIER | c.-1529G>A| |
S112 |
| 171375 | BAA02g15610 | A02 | 7545566 | G | A | upstream_gene_variant | MODIFIER | c.-2009C>T| |
S187 |