| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 179951 | BAA02g20090 | A02 | 10596230 | C | T | missense_variant | MODERATE | c.866C>T|p.Ser289Phe |
S166 |
| 179952 | BAA02g20090 | A02 | 10598022 | G | A | downstream_gene_variant | MODIFIER | c.*1614G>A| |
S188 |
| 179953 | BAA02g20090 | A02 | 10598212 | C | T | downstream_gene_variant | MODIFIER | c.*1804C>T| |
S49 |
| 179954 | BAA02g20090 | A02 | 10598230 | C | T | downstream_gene_variant | MODIFIER | c.*1822C>T| |
S182 |
| 179955 | BAA02g20090 | A02 | 10598502 | C | T | downstream_gene_variant | MODIFIER | c.*2094C>T| |
S9 |
| 179956 | BAA02g20090 | A02 | 10598531 | G | A | downstream_gene_variant | MODIFIER | c.*2123G>A| |
S223 |
| 179957 | BAA02g20090 | A02 | 10598994 | C | T | downstream_gene_variant | MODIFIER | c.*2586C>T| |
S25 |
| 179958 | BAA02g20090 | A02 | 10599051 | G | A | downstream_gene_variant | MODIFIER | c.*2643G>A| |
S193 |
| 179959 | BAA02g20090 | A02 | 10599388 | C | T | downstream_gene_variant | MODIFIER | c.*2980C>T| |
S211 S227 |
| 179960 | BAA02g20090 | A02 | 10599412 | A | C | downstream_gene_variant | MODIFIER | c.*3004A>C| |
S269 |
| 179961 | BAA02g20090 | A02 | 10599678 | C | T | downstream_gene_variant | MODIFIER | c.*3270C>T| |
S143 |
| 179962 | BAA02g20090 | A02 | 10599707 | G | A | downstream_gene_variant | MODIFIER | c.*3299G>A| |
S170 |
| 179963 | BAA02g20090 | A02 | 10600251 | C | T | downstream_gene_variant | MODIFIER | c.*3843C>T| |
S120 |
| 179964 | BAA02g20100 | A02 | 10600978 | G | A | synonymous_variant | LOW | c.2553C>T|p.Asn851Asn |
S19 |
| 179965 | BAA02g20100 | A02 | 10601116 | G | A | synonymous_variant | LOW | c.2415C>T|p.Pro805Pro |
S67 |
| 179966 | BAA02g20100 | A02 | 10601516 | G | A | missense_variant | MODERATE | c.2015C>T|p.Ser672Phe |
S159 S243 |
| 179967 | BAA02g20100 | A02 | 10601711 | G | A | missense_variant | MODERATE | c.1820C>T|p.Ser607Phe |
S264 |
| 179968 | BAA02g20100 | A02 | 10602542 | C | T | missense_variant | MODERATE | c.1075G>A|p.Asp359Asn |
S75 S81 |
| 179969 | BAA02g20100 | A02 | 10602741 | C | T | synonymous_variant | LOW | c.876G>A|p.Gln292Gln |
S108 |
| 179970 | BAA02g20100 | A02 | 10603626 | C | T | upstream_gene_variant | MODIFIER | c.-10G>A| |
S277 |
| 179971 | BAA02g20100 | A02 | 10605632 | C | T | upstream_gene_variant | MODIFIER | c.-2016G>A| |
S184 |
| 179972 | BAA02g20100 | A02 | 10606144 | C | T | upstream_gene_variant | MODIFIER | c.-2528G>A| |
S267 |
| 179973 | BAA02g20100 | A02 | 10607087 | C | T | upstream_gene_variant | MODIFIER | c.-3471G>A| |
S32 |
| 179974 | BAA02g20110 | A02 | 10609521 | C | T | upstream_gene_variant | MODIFIER | c.-2972G>A| |
S54 |
| 179975 | BAA02g20110 | A02 | 10610405 | G | A | upstream_gene_variant | MODIFIER | c.-3856C>T| |
S200 |