| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 139251 | BAA10g24530 | A10 | 20177681 | G | A | synonymous_variant | LOW | c.606C>T|p.Val202Val |
S149 S176 |
| 139252 | BAA10g24530 | A10 | 20179501 | C | T | upstream_gene_variant | MODIFIER | c.-793G>A| |
S48 |
| 139253 | BAA10g24530 | A10 | 20179949 | C | T | upstream_gene_variant | MODIFIER | c.-1241G>A| |
S247 |
| 139254 | BAA10g24540 | A10 | 20180121 | C | T | splice_region_variant&intron_variant | LOW | c.970-8G>A| |
S42 |
| 139255 | BAA10g24530 | A10 | 20181384 | C | T | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S87 |
| 139256 | BAA10g24540 | A10 | 20186496 | G | A | upstream_gene_variant | MODIFIER | c.-2720C>T| |
S270 |
| 139257 | BAA10g24540 | A10 | 20186582 | G | A | upstream_gene_variant | MODIFIER | c.-2806C>T| |
S156 |
| 139258 | BAA10g24540 | A10 | 20187954 | C | T | upstream_gene_variant | MODIFIER | c.-4178G>A| |
S275 |
| 139259 | BAA10g24560 | A10 | 20188741 | G | A | missense_variant | MODERATE | c.100C>T|p.Leu34Phe |
S228 |
| 139260 | BAA10g24550 | A10 | 20189100 | G | A | upstream_gene_variant | MODIFIER | c.-3461C>T| |
S69 |
| 139261 | BAA10g24550 | A10 | 20189947 | T | A | upstream_gene_variant | MODIFIER | c.-4308A>T| |
S251 |
| 139262 | BAA10g24550 | A10 | 20190347 | C | T | upstream_gene_variant | MODIFIER | c.-4708G>A| |
S257 |
| 139263 | BAA10g24550 | A10 | 20190421 | G | A | upstream_gene_variant | MODIFIER | c.-4782C>T| |
S182 |
| 139264 | BAA10g24550 | A10 | 20190521 | G | A | upstream_gene_variant | MODIFIER | c.-4882C>T| |
S66 |
| 139265 | BAA10g24570 | A10 | 20191185 | G | A | missense_variant | MODERATE | c.755C>T|p.Thr252Met |
S179 |
| 139266 | BAA10g24560 | A10 | 20191401 | T | C | upstream_gene_variant | MODIFIER | c.-2449A>G| |
S76 |
| 139267 | BAA10g24570 | A10 | 20191513 | C | T | missense_variant | MODERATE | c.539G>A|p.Gly180Glu |
S296 |
| 139268 | BAA10g24570 | A10 | 20191703 | C | T | missense_variant | MODERATE | c.349G>A|p.Val117Ile |
S221 |
| 139269 | BAA10g24570 | A10 | 20192096 | C | T | missense_variant | MODERATE | c.43G>A|p.Gly15Arg |
S211 S227 |
| 139270 | BAA10g24560 | A10 | 20192377 | C | T | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S10 |
| 139271 | BAA10g24560 | A10 | 20192526 | G | A | upstream_gene_variant | MODIFIER | c.-3574C>T| |
S293 |
| 139272 | BAA10g24570 | A10 | 20194519 | G | A | upstream_gene_variant | MODIFIER | c.-2381C>T| |
S209 |
| 139273 | BAA10g24580 | A10 | 20200574 | G | A | missense_variant | MODERATE | c.8G>A|p.Arg3Lys |
S17 |
| 139274 | BAA10g24580 | A10 | 20203972 | C | T | downstream_gene_variant | MODIFIER | c.*1792C>T| |
S33 |
| 139275 | BAA10g24590 | A10 | 20205255 | G | A | upstream_gene_variant | MODIFIER | c.-547C>T| |
S179 |