| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141451 | BAA10g26490 | A10 | 20986030 | C | T | splice_donor_variant&intron_variant | HIGH | c.1320+1G>A| |
S152 |
| 141452 | BAA10g26480 | A10 | 20986718 | C | T | upstream_gene_variant | MODIFIER | c.-2376G>A| |
S238 |
| 141453 | BAA10g26480 | A10 | 20986723 | C | T | upstream_gene_variant | MODIFIER | c.-2381G>A| |
S106 |
| 141454 | BAA10g26480 | A10 | 20988303 | C | T | upstream_gene_variant | MODIFIER | c.-3961G>A| |
S56 |
| 141455 | BAA10g26500 | A10 | 20989537 | C | T | missense_variant&splice_region_variant | MODERATE | c.1349G>A|p.Gly450Glu |
S46 |
| 141456 | BAA10g26500 | A10 | 20989825 | C | T | synonymous_variant | LOW | c.1152G>A|p.Thr384Thr |
S272 |
| 141457 | BAA10g26500 | A10 | 20990952 | G | A | synonymous_variant | LOW | c.627C>T|p.His209His |
S139 |
| 141458 | BAA10g26490 | A10 | 20991121 | G | A | upstream_gene_variant | MODIFIER | c.-3204C>T| |
S179 |
| 141459 | BAA10g26490 | A10 | 20992364 | G | A | upstream_gene_variant | MODIFIER | c.-4447C>T| |
S298 |
| 141460 | BAA10g26500 | A10 | 20994435 | C | T | upstream_gene_variant | MODIFIER | c.-2411G>A| |
S242 |
| 141461 | BAA10g26500 | A10 | 20994901 | C | T | upstream_gene_variant | MODIFIER | c.-2877G>A| |
S269 |
| 141462 | BAA10g26500 | A10 | 20995088 | C | T | upstream_gene_variant | MODIFIER | c.-3064G>A| |
S221 |
| 141463 | BAA10g26500 | A10 | 20995243 | C | T | upstream_gene_variant | MODIFIER | c.-3219G>A| |
S166 |
| 141464 | BAA10g26500 | A10 | 20995686 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S277 |
| 141465 | BAA10g26500 | A10 | 20996451 | C | T | upstream_gene_variant | MODIFIER | c.-4427G>A| |
S247 |
| 141466 | BAA10g26500 | A10 | 20996630 | C | T | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S177 |
| 141467 | BAA10g26510 | A10 | 20997741 | C | T | missense_variant | MODERATE | c.1085G>A|p.Arg362Gln |
S25 |
| 141468 | BAA10g26510 | A10 | 20997991 | G | A | missense_variant | MODERATE | c.835C>T|p.Leu279Phe |
S178 |
| 141469 | BAA10g26510 | A10 | 20998020 | C | T | missense_variant | MODERATE | c.806G>A|p.Gly269Asp |
S133 |
| 141470 | BAA10g26520 | A10 | 20998161 | C | T | upstream_gene_variant | MODIFIER | c.-2332C>T| |
S210 S225 |
| 141471 | BAA10g26510 | A10 | 20999271 | C | T | missense_variant | MODERATE | c.64G>A|p.Ala22Thr |
S292 |
| 141472 | BAA10g26510 | A10 | 20999689 | G | A | upstream_gene_variant | MODIFIER | c.-355C>T| |
S183 |
| 141473 | BAA10g26510 | A10 | 21000089 | C | T | upstream_gene_variant | MODIFIER | c.-755G>A| |
S229 |
| 141474 | BAA10g26510 | A10 | 21002031 | C | T | upstream_gene_variant | MODIFIER | c.-2697G>A| |
S14 |
| 141475 | BAA10g26510 | A10 | 21002040 | T | A | upstream_gene_variant | MODIFIER | c.-2706A>T| |
S138 |