Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
4501 | BAA01g03620 | A01 | 1641695 | C | T | intron_variant | MODIFIER | c.3142-67C>T| |
S206 S26 |
4502 | BAA01g03620 | A01 | 1641789 | C | T | missense_variant | MODERATE | c.3169C>T|p.Arg1057Cys |
S127 |
4503 | BAA01g03620 | A01 | 1641977 | G | A | intron_variant | MODIFIER | c.3259-46G>A| |
S115 |
4504 | BAA01g03620 | A01 | 1642601 | C | T | synonymous_variant | LOW | c.3837C>T|p.Cys1279Cys |
S58 |
4505 | BAA01g03620 | A01 | 1642779 | G | A | missense_variant | MODERATE | c.4015G>A|p.Glu1339Lys |
S180 |
4506 | BAA01g03620 | A01 | 1643231 | C | T | downstream_gene_variant | MODIFIER | c.*69C>T| |
S47 |
4507 | BAA01g03620 | A01 | 1643323 | G | A | downstream_gene_variant | MODIFIER | c.*161G>A| |
S293 |
4508 | BAA01g03620 | A01 | 1644214 | G | A | downstream_gene_variant | MODIFIER | c.*1052G>A| |
S123 |
4509 | BAA01g03620 | A01 | 1644323 | C | T | downstream_gene_variant | MODIFIER | c.*1161C>T| |
S205 |
4510 | BAA01g03620 | A01 | 1645021 | G | A | downstream_gene_variant | MODIFIER | c.*1859G>A| |
S98 |
4511 | BAA01g03620 | A01 | 1645728 | G | A | downstream_gene_variant | MODIFIER | c.*2566G>A| |
S251 |
4512 | BAA01g03620 | A01 | 1646334 | C | T | downstream_gene_variant | MODIFIER | c.*3172C>T| |
S20 |
4513 | BAA01g03630 | A01 | 1651669 | G | A | missense_variant | MODERATE | c.191C>T|p.Pro64Leu |
S293 |
4514 | BAA01g03630 | A01 | 1652931 | G | A | upstream_gene_variant | MODIFIER | c.-1072C>T| |
S118 |
4515 | BAA01g03640 | A01 | 1654287 | C | T | missense_variant | MODERATE | c.514G>A|p.Ala172Thr |
S150 |
4516 | BAA01g03630 | A01 | 1654338 | G | A | upstream_gene_variant | MODIFIER | c.-2479C>T| |
S10 |
4517 | BAA01g03640 | A01 | 1655724 | G | A | missense_variant | MODERATE | c.59C>T|p.Thr20Ile |
S38 |
4518 | BAA01g03630 | A01 | 1656441 | G | A | upstream_gene_variant | MODIFIER | c.-4582C>T| |
S219 S72 |
4519 | BAA01g03640 | A01 | 1657162 | G | A | upstream_gene_variant | MODIFIER | c.-1380C>T| |
S142 |
4520 | BAA01g03650 | A01 | 1657509 | C | T | synonymous_variant | LOW | c.270C>T|p.Phe90Phe |
S87 |
4521 | BAA01g03650 | A01 | 1659299 | G | A | missense_variant | MODERATE | c.1168G>A|p.Glu390Lys |
S294 |
4522 | BAA01g03650 | A01 | 1660398 | G | A | missense_variant | MODERATE | c.1828G>A|p.Glu610Lys |
S175 |
4523 | BAA01g03650 | A01 | 1660553 | G | A | synonymous_variant | LOW | c.1983G>A|p.Lys661Lys |
S122 |
4524 | BAA01g03640 | A01 | 1660630 | C | T | upstream_gene_variant | MODIFIER | c.-4848G>A| |
S25 |
4525 | BAA01g03650 | A01 | 1661229 | C | T | downstream_gene_variant | MODIFIER | c.*443C>T| |
S25 |