| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 139351 | BAA10g24630 | A10 | 20217852 | C | T | synonymous_variant | LOW | c.252C>T|p.Ala84Ala |
S11 |
| 139352 | BAA10g24630 | A10 | 20218053 | C | T | synonymous_variant | LOW | c.453C>T|p.Asp151Asp |
S148 S30 S31 |
| 139353 | BAA10g24630 | A10 | 20218461 | G | A | missense_variant | MODERATE | c.779G>A|p.Gly260Glu |
S280 |
| 139354 | BAA10g24630 | A10 | 20218499 | G | A | missense_variant | MODERATE | c.817G>A|p.Glu273Lys |
S273 |
| 139355 | BAA10g24640 | A10 | 20219018 | G | A | upstream_gene_variant | MODIFIER | c.-1843G>A| |
S62 |
| 139356 | BAA10g24630 | A10 | 20219168 | C | T | synonymous_variant | LOW | c.1236C>T|p.Ser412Ser |
S204 |
| 139357 | BAA10g24630 | A10 | 20219625 | G | A | missense_variant | MODERATE | c.1615G>A|p.Ala539Thr |
S139 |
| 139358 | BAA10g24640 | A10 | 20220617 | G | A | upstream_gene_variant | MODIFIER | c.-244G>A| |
S67 |
| 139359 | BAA10g24640 | A10 | 20220773 | G | A | upstream_gene_variant | MODIFIER | c.-88G>A| |
S272 |
| 139360 | BAA10g24640 | A10 | 20221108 | C | T | missense_variant | MODERATE | c.248C>T|p.Thr83Met |
S33 |
| 139361 | BAA10g24640 | A10 | 20223139 | C | T | missense_variant | MODERATE | c.1514C>T|p.Pro505Leu |
S140 |
| 139362 | BAA10g24640 | A10 | 20223153 | G | A | missense_variant | MODERATE | c.1528G>A|p.Glu510Lys |
S139 |
| 139363 | BAA10g24650 | A10 | 20225789 | C | T | upstream_gene_variant | MODIFIER | c.-3952C>T| |
S204 |
| 139364 | BAA10g24640 | A10 | 20226852 | G | A | missense_variant | MODERATE | c.2098G>A|p.Gly700Arg |
S293 |
| 139365 | BAA10g24650 | A10 | 20228420 | C | T | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S133 |
| 139366 | BAA10g24650 | A10 | 20228592 | G | A | upstream_gene_variant | MODIFIER | c.-1149G>A| |
S134 |
| 139367 | BAA10g24650 | A10 | 20229818 | G | A | synonymous_variant | LOW | c.78G>A|p.Arg26Arg |
S192 |
| 139368 | BAA10g24650 | A10 | 20230004 | C | T | synonymous_variant | LOW | c.264C>T|p.Asp88Asp |
S269 |
| 139369 | BAA10g24650 | A10 | 20230110 | C | T | missense_variant | MODERATE | c.370C>T|p.Pro124Ser |
S157 |
| 139370 | BAA10g24650 | A10 | 20230503 | C | T | missense_variant | MODERATE | c.763C>T|p.Pro255Ser |
S229 |
| 139371 | BAA10g24660 | A10 | 20231037 | G | A | upstream_gene_variant | MODIFIER | c.-575G>A| |
S261 |
| 139372 | BAA10g24670 | A10 | 20233250 | C | T | upstream_gene_variant | MODIFIER | c.-1289C>T| |
S34 |
| 139373 | BAA10g24680 | A10 | 20235633 | C | T | missense_variant | MODERATE | c.1129G>A|p.Glu377Lys |
S119 |
| 139374 | BAA10g24660 | A10 | 20236299 | C | T | downstream_gene_variant | MODIFIER | c.*3796C>T| |
S114 |
| 139375 | BAA10g24680 | A10 | 20236550 | C | T | splice_region_variant&intron_variant | LOW | c.829-8G>A| |
S8 |