| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 176651 | BAA02g18480 | A02 | 9426428 | G | A | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S4 |
| 176652 | BAA02g18480 | A02 | 9426729 | C | T | upstream_gene_variant | MODIFIER | c.-3466G>A| |
S302 |
| 176653 | BAA02g18480 | A02 | 9426779 | G | A | upstream_gene_variant | MODIFIER | c.-3516C>T| |
S197 |
| 176654 | BAA02g18480 | A02 | 9426912 | C | T | upstream_gene_variant | MODIFIER | c.-3649G>A| |
S293 |
| 176655 | BAA02g18480 | A02 | 9427353 | G | A | upstream_gene_variant | MODIFIER | c.-4090C>T| |
S153 S213 |
| 176656 | BAA02g18480 | A02 | 9427403 | C | T | upstream_gene_variant | MODIFIER | c.-4140G>A| |
S100 |
| 176657 | BAA02g18480 | A02 | 9427761 | C | T | upstream_gene_variant | MODIFIER | c.-4498G>A| |
S289 S290 |
| 176658 | BAA02g18480 | A02 | 9427826 | G | A | upstream_gene_variant | MODIFIER | c.-4563C>T| |
S287 |
| 176659 | BAA02g18480 | A02 | 9428132 | C | T | upstream_gene_variant | MODIFIER | c.-4869G>A| |
S302 |
| 176660 | BAA02g18490 | A02 | 9428419 | C | T | upstream_gene_variant | MODIFIER | c.-1253C>T| |
S244 |
| 176661 | BAA02g18490 | A02 | 9429165 | C | T | upstream_gene_variant | MODIFIER | c.-507C>T| |
S183 S198 |
| 176662 | BAA02g18490 | A02 | 9430117 | C | T | missense_variant | MODERATE | c.310C>T|p.Arg104Cys |
S283 |
| 176663 | BAA02g18500 | A02 | 9432128 | C | T | upstream_gene_variant | MODIFIER | c.-108G>A| |
S233 |
| 176664 | BAA02g18500 | A02 | 9434239 | C | T | upstream_gene_variant | MODIFIER | c.-2219G>A| |
S163 |
| 176665 | BAA02g18520 | A02 | 9435324 | G | A | synonymous_variant | LOW | c.1831C>T|p.Leu611Leu |
S293 |
| 176666 | BAA02g18520 | A02 | 9436957 | C | T | splice_region_variant&intron_variant | LOW | c.1387+5G>A| |
S292 |
| 176667 | BAA02g18520 | A02 | 9437226 | C | T | missense_variant | MODERATE | c.1123G>A|p.Gly375Ser |
S245 |
| 176668 | BAA02g18520 | A02 | 9437501 | C | T | missense_variant | MODERATE | c.848G>A|p.Arg283Lys |
S46 |
| 176669 | BAA02g18520 | A02 | 9437610 | G | A | missense_variant | MODERATE | c.739C>T|p.Leu247Phe |
S264 |
| 176670 | BAA02g18520 | A02 | 9438592 | C | T | missense_variant | MODERATE | c.211G>A|p.Glu71Lys |
S200 |
| 176671 | BAA02g18520 | A02 | 9438841 | C | T | upstream_gene_variant | MODIFIER | c.-39G>A| |
S301 S304 |
| 176672 | BAA02g18520 | A02 | 9439511 | G | A | upstream_gene_variant | MODIFIER | c.-709C>T| |
S132 S137 S215 |
| 176673 | BAA02g18530 | A02 | 9439970 | C | T | stop_gained | HIGH | c.58C>T|p.Gln20* |
S283 |
| 176674 | BAA02g18520 | A02 | 9440111 | C | T | upstream_gene_variant | MODIFIER | c.-1309G>A| |
S249 |
| 176675 | BAA02g18530 | A02 | 9440324 | C | T | splice_region_variant&synonymous_variant | LOW | c.208C>T|p.Leu70Leu |
S105 S106 |