| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141251 | BAA10g26270 | A10 | 20903502 | G | A | upstream_gene_variant | MODIFIER | c.-543C>T| |
S71 |
| 141252 | BAA10g26270 | A10 | 20904057 | C | T | upstream_gene_variant | MODIFIER | c.-1098G>A| |
S206 S26 |
| 141253 | BAA10g26280 | A10 | 20904257 | C | T | synonymous_variant | LOW | c.90C>T|p.Ala30Ala |
S28 |
| 141254 | BAA10g26280 | A10 | 20905065 | G | A | synonymous_variant | LOW | c.663G>A|p.Lys221Lys |
S245 |
| 141255 | BAA10g26280 | A10 | 20905618 | C | T | stop_gained | HIGH | c.958C>T|p.Gln320* |
S174 S216 S241 S27 |
| 141256 | BAA10g26270 | A10 | 20907797 | C | T | upstream_gene_variant | MODIFIER | c.-4838G>A| |
S287 |
| 141257 | BAA10g26280 | A10 | 20908911 | G | A | downstream_gene_variant | MODIFIER | c.*2903G>A| |
S132 S137 S215 |
| 141258 | BAA10g26290 | A10 | 20909251 | C | T | splice_region_variant&intron_variant | LOW | c.630+7C>T| |
S153 S213 |
| 141259 | BAA10g26290 | A10 | 20909386 | G | A | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S164 |
| 141260 | BAA10g26290 | A10 | 20911385 | G | A | synonymous_variant | LOW | c.1572G>A|p.Leu524Leu |
S67 |
| 141261 | BAA10g26290 | A10 | 20913025 | C | T | intron_variant | MODIFIER | c.2513+15C>T| |
S133 |
| 141262 | BAA10g26290 | A10 | 20913283 | G | A | missense_variant | MODERATE | c.2645G>A|p.Arg882Lys |
S67 |
| 141263 | BAA10g26290 | A10 | 20914794 | C | T | missense_variant | MODERATE | c.3476C>T|p.Ala1159Val |
S155 S211 |
| 141264 | BAA10g26290 | A10 | 20914936 | C | T | synonymous_variant | LOW | c.3546C>T|p.Leu1182Leu |
S206 S26 |
| 141265 | BAA10g26300 | A10 | 20915298 | G | A | upstream_gene_variant | MODIFIER | c.-4057G>A| |
S192 |
| 141266 | BAA10g26300 | A10 | 20915979 | C | T | upstream_gene_variant | MODIFIER | c.-3376C>T| |
S92 |
| 141267 | BAA10g26290 | A10 | 20916634 | C | T | splice_region_variant&intron_variant | LOW | c.4584+4C>T| |
S168 |
| 141268 | BAA10g26290 | A10 | 20916893 | G | A | missense_variant | MODERATE | c.4769G>A|p.Gly1590Glu |
S63 |
| 141269 | BAA10g26290 | A10 | 20917453 | C | T | stop_gained | HIGH | c.5329C>T|p.Gln1777* |
S8 |
| 141270 | BAA10g26290 | A10 | 20917491 | G | A | synonymous_variant | LOW | c.5367G>A|p.Arg1789Arg |
S256 |
| 141271 | BAA10g26310 | A10 | 20920511 | C | T | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S260 |
| 141272 | BAA10g26310 | A10 | 20920891 | C | T | upstream_gene_variant | MODIFIER | c.-962C>T| |
S292 |
| 141273 | BAA10g26310 | A10 | 20921641 | C | T | upstream_gene_variant | MODIFIER | c.-212C>T| |
S130 |
| 141274 | BAA10g26290 | A10 | 20922495 | G | T | downstream_gene_variant | MODIFIER | c.*4251G>T| |
|
| 141275 | BAA10g26300 | A10 | 20923356 | C | T | downstream_gene_variant | MODIFIER | c.*3393C>T| |
S12 |