| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 87401 | BAA01g46580 | A01 | 31019104 | C | T | synonymous_variant | LOW | c.43C>T|p.Leu15Leu |
S43 |
| 87402 | BAA01g46580 | A01 | 31019151 | G | A | synonymous_variant | LOW | c.90G>A|p.Ala30Ala |
S162 |
| 87403 | BAA01g46570 | A01 | 31020261 | G | A | upstream_gene_variant | MODIFIER | c.-4553C>T| |
S4 |
| 87404 | BAA01g46580 | A01 | 31020430 | G | A | missense_variant | MODERATE | c.677G>A|p.Ser226Asn |
S274 |
| 87405 | BAA01g46580 | A01 | 31020773 | C | T | missense_variant | MODERATE | c.833C>T|p.Pro278Leu |
S43 |
| 87406 | BAA01g46590 | A01 | 31022050 | G | A | missense_variant | MODERATE | c.1100C>T|p.Ser367Leu |
S130 |
| 87407 | BAA01g46580 | A01 | 31022513 | G | A | downstream_gene_variant | MODIFIER | c.*1138G>A| |
S201 |
| 87408 | BAA01g46590 | A01 | 31022927 | G | A | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S273 |
| 87409 | BAA01g46590 | A01 | 31022967 | C | T | missense_variant | MODERATE | c.403G>A|p.Gly135Ser |
S194 S217 |
| 87410 | BAA01g46590 | A01 | 31023027 | C | T | missense_variant | MODERATE | c.343G>A|p.Val115Ile |
S139 |
| 87411 | BAA01g46590 | A01 | 31023375 | C | T | synonymous_variant | LOW | c.72G>A|p.Val24Val |
S280 |
| 87412 | BAA01g46590 | A01 | 31023405 | C | T | synonymous_variant | LOW | c.42G>A|p.Pro14Pro |
S296 |
| 87413 | BAA01g46590 | A01 | 31024506 | C | T | upstream_gene_variant | MODIFIER | c.-1060G>A| |
S244 |
| 87414 | BAA01g46590 | A01 | 31025337 | G | A | upstream_gene_variant | MODIFIER | c.-1891C>T| |
S201 |
| 87415 | BAA01g46590 | A01 | 31025474 | G | A | upstream_gene_variant | MODIFIER | c.-2028C>T| |
S111 |
| 87416 | BAA01g46590 | A01 | 31025838 | G | A | upstream_gene_variant | MODIFIER | c.-2392C>T| |
S260 |
| 87417 | BAA01g46590 | A01 | 31028278 | C | T | upstream_gene_variant | MODIFIER | c.-4832G>A| |
S293 |
| 87418 | BAA01g46600 | A01 | 31029002 | G | A | synonymous_variant | LOW | c.486C>T|p.Ala162Ala |
S192 |
| 87419 | BAA01g46600 | A01 | 31029887 | C | T | missense_variant | MODERATE | c.122G>A|p.Arg41Lys |
S155 S211 |
| 87420 | BAA01g46600 | A01 | 31033656 | G | A | upstream_gene_variant | MODIFIER | c.-3474C>T| |
S230 |
| 87421 | BAA01g46600 | A01 | 31034237 | C | T | upstream_gene_variant | MODIFIER | c.-4055G>A| |
S169 |
| 87422 | BAA01g46610 | A01 | 31035876 | C | T | missense_variant | MODERATE | c.194G>A|p.Arg65Lys |
S228 |
| 87423 | BAA01g46620 | A01 | 31036305 | C | T | downstream_gene_variant | MODIFIER | c.*988G>A| |
S15 S3 |
| 87424 | BAA01g46610 | A01 | 31036545 | C | T | missense_variant&splice_region_variant | MODERATE | c.184G>A|p.Gly62Ser |
S295 |
| 87425 | BAA01g46610 | A01 | 31037139 | G | A | upstream_gene_variant | MODIFIER | c.-411C>T| |
S240 |