| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 76401 | BAA01g40330 | A01 | 26757020 | C | T | upstream_gene_variant | MODIFIER | c.-537C>T| |
S88 |
| 76402 | BAA01g40330 | A01 | 26757591 | C | T | missense_variant | MODERATE | c.35C>T|p.Pro12Leu |
S256 |
| 76403 | BAA01g40330 | A01 | 26758163 | G | A | missense_variant | MODERATE | c.607G>A|p.Glu203Lys |
S126 |
| 76404 | BAA01g40330 | A01 | 26758662 | C | T | missense_variant | MODERATE | c.1106C>T|p.Thr369Ile |
S192 |
| 76405 | BAA01g40330 | A01 | 26758771 | G | A | stop_gained | HIGH | c.1215G>A|p.Trp405* |
S204 |
| 76406 | BAA01g40330 | A01 | 26759008 | C | T | synonymous_variant | LOW | c.1452C>T|p.Phe484Phe |
S59 |
| 76407 | BAA01g40330 | A01 | 26759102 | G | A | missense_variant | MODERATE | c.1546G>A|p.Ala516Thr |
S149 |
| 76408 | BAA01g40330 | A01 | 26759763 | C | T | missense_variant | MODERATE | c.2207C>T|p.Ala736Val |
S292 |
| 76409 | BAA01g40330 | A01 | 26760357 | G | A | missense_variant | MODERATE | c.2652G>A|p.Met884Ile |
S296 |
| 76410 | BAA01g40330 | A01 | 26760766 | C | T | missense_variant | MODERATE | c.2984C>T|p.Ser995Phe |
S78 S83 |
| 76411 | BAA01g40330 | A01 | 26761728 | G | A | missense_variant | MODERATE | c.3644G>A|p.Ser1215Asn |
S114 |
| 76412 | BAA01g40330 | A01 | 26761830 | G | A | missense_variant | MODERATE | c.3746G>A|p.Gly1249Glu |
S126 |
| 76413 | BAA01g40340 | A01 | 26763432 | C | T | missense_variant | MODERATE | c.67C>T|p.Leu23Phe |
S157 |
| 76414 | BAA01g40340 | A01 | 26764098 | C | T | synonymous_variant | LOW | c.733C>T|p.Leu245Leu |
S216 |
| 76415 | BAA01g40340 | A01 | 26764758 | G | A | missense_variant | MODERATE | c.1393G>A|p.Glu465Lys |
S295 |
| 76416 | BAA01g40340 | A01 | 26764958 | C | T | synonymous_variant | LOW | c.1593C>T|p.Val531Val |
S182 |
| 76417 | BAA01g40340 | A01 | 26764992 | C | T | missense_variant | MODERATE | c.1627C>T|p.Pro543Ser |
S230 |
| 76418 | BAA01g40340 | A01 | 26765239 | C | T | missense_variant | MODERATE | c.1874C>T|p.Pro625Leu |
S12 |
| 76419 | BAA01g40340 | A01 | 26765417 | G | A | synonymous_variant | LOW | c.2052G>A|p.Gln684Gln |
S232 |
| 76420 | BAA01g40340 | A01 | 26765754 | G | A | missense_variant&splice_region_variant | MODERATE | c.2323G>A|p.Glu775Lys |
S104 |
| 76421 | BAA01g40340 | A01 | 26766375 | G | A | missense_variant | MODERATE | c.2866G>A|p.Val956Met |
S172 S217 |
| 76422 | BAA01g40340 | A01 | 26766716 | G | A | synonymous_variant | LOW | c.3123G>A|p.Gly1041Gly |
S20 |
| 76423 | BAA01g40340 | A01 | 26768135 | G | A | missense_variant | MODERATE | c.4294G>A|p.Asp1432Asn |
S179 |
| 76424 | BAA01g40340 | A01 | 26768156 | C | T | missense_variant | MODERATE | c.4315C>T|p.Leu1439Phe |
S62 |
| 76425 | BAA01g40350 | A01 | 26769689 | G | A | missense_variant | MODERATE | c.1382C>T|p.Ser461Phe |
S13 |