| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 76251 | BAA01g40140 | A01 | 26704359 | C | T | upstream_gene_variant | MODIFIER | c.-3095G>A| |
S69 |
| 76252 | BAA01g40150 | A01 | 26704997 | G | A | synonymous_variant | LOW | c.261G>A|p.Arg87Arg |
S87 |
| 76253 | BAA01g40150 | A01 | 26705036 | G | A | synonymous_variant | LOW | c.300G>A|p.Ser100Ser |
S79 |
| 76254 | BAA01g40170 | A01 | 26706684 | G | A | missense_variant | MODERATE | c.49G>A|p.Val17Met |
S245 |
| 76255 | BAA01g40160 | A01 | 26707753 | G | A | upstream_gene_variant | MODIFIER | c.-1479C>T| |
S129 S34 |
| 76256 | BAA01g40180 | A01 | 26708761 | G | A | missense_variant | MODERATE | c.413G>A|p.Arg138Lys |
S179 |
| 76257 | BAA01g40180 | A01 | 26710134 | C | T | synonymous_variant | LOW | c.960C>T|p.Asp320Asp |
S210 S225 |
| 76258 | BAA01g40180 | A01 | 26710473 | G | A | missense_variant | MODERATE | c.1108G>A|p.Glu370Lys |
S265 |
| 76259 | BAA01g40180 | A01 | 26710510 | C | T | missense_variant | MODERATE | c.1145C>T|p.Ser382Phe |
S210 S225 |
| 76260 | BAA01g40190 | A01 | 26712993 | C | T | missense_variant | MODERATE | c.1052C>T|p.Ala351Val |
S303 |
| 76261 | BAA01g40210 | A01 | 26713376 | C | T | upstream_gene_variant | MODIFIER | c.-3211C>T| |
S52 |
| 76262 | BAA01g40210 | A01 | 26716881 | G | A | missense_variant | MODERATE | c.100G>A|p.Asp34Asn |
S208 |
| 76263 | BAA01g40210 | A01 | 26718381 | C | T | synonymous_variant | LOW | c.1024C>T|p.Leu342Leu |
S53 |
| 76264 | BAA01g40210 | A01 | 26718472 | G | A | synonymous_variant | LOW | c.1041G>A|p.Gly347Gly |
S152 |
| 76265 | BAA01g40210 | A01 | 26718672 | C | T | missense_variant | MODERATE | c.1241C>T|p.Ala414Val |
S162 |
| 76266 | BAA01g40210 | A01 | 26718694 | C | T | synonymous_variant | LOW | c.1263C>T|p.Pro421Pro |
S281 |
| 76267 | BAA01g40210 | A01 | 26718772 | C | T | synonymous_variant | LOW | c.1341C>T|p.Ser447Ser |
S17 |
| 76268 | BAA01g40210 | A01 | 26718932 | G | A | missense_variant | MODERATE | c.1501G>A|p.Glu501Lys |
S163 |
| 76269 | BAA01g40210 | A01 | 26719025 | G | A | missense_variant | MODERATE | c.1594G>A|p.Glu532Lys |
S61 |
| 76270 | BAA01g40210 | A01 | 26719103 | C | T | missense_variant | MODERATE | c.1672C>T|p.Pro558Ser |
S193 |
| 76271 | BAA01g40210 | A01 | 26719295 | C | T | stop_gained | HIGH | c.1864C>T|p.Gln622* |
S282 |
| 76272 | BAA01g40210 | A01 | 26719305 | G | A | missense_variant | MODERATE | c.1874G>A|p.Gly625Glu |
S278 |
| 76273 | BAA01g40210 | A01 | 26720206 | G | A | missense_variant | MODERATE | c.2462G>A|p.Gly821Glu |
S191 |
| 76274 | BAA01g40230 | A01 | 26722074 | G | A | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S245 |
| 76275 | BAA01g40230 | A01 | 26722688 | C | T | upstream_gene_variant | MODIFIER | c.-3790C>T| |
S77 |