| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 129651 | BAA10g17500 | A10 | 16808904 | G | A | downstream_gene_variant | MODIFIER | c.*582C>T| |
S59 |
| 129652 | BAA10g17500 | A10 | 16809000 | G | A | downstream_gene_variant | MODIFIER | c.*486C>T| |
S172 S176 S202 S217 |
| 129653 | BAA10g17500 | A10 | 16809134 | G | A | downstream_gene_variant | MODIFIER | c.*352C>T| |
S302 |
| 129654 | BAA10g17500 | A10 | 16809141 | C | T | downstream_gene_variant | MODIFIER | c.*345G>A| |
S193 |
| 129655 | BAA10g17510 | A10 | 16810087 | G | A | downstream_gene_variant | MODIFIER | c.*4264C>T| |
S298 |
| 129656 | BAA10g17510 | A10 | 16810123 | C | T | downstream_gene_variant | MODIFIER | c.*4228G>A| |
S123 |
| 129657 | BAA10g17510 | A10 | 16810275 | C | T | downstream_gene_variant | MODIFIER | c.*4076G>A| |
S45 |
| 129658 | BAA10g17510 | A10 | 16811705 | G | A | downstream_gene_variant | MODIFIER | c.*2646C>T| |
S251 |
| 129659 | BAA10g17500 | A10 | 16812745 | G | A | synonymous_variant | LOW | c.99C>T|p.Phe33Phe |
S138 |
| 129660 | BAA10g17500 | A10 | 16812923 | C | T | upstream_gene_variant | MODIFIER | c.-80G>A| |
S15 S156 S3 S34 |
| 129661 | BAA10g17500 | A10 | 16813122 | G | A | upstream_gene_variant | MODIFIER | c.-279C>T| |
S195 |
| 129662 | BAA10g17500 | A10 | 16813471 | C | T | upstream_gene_variant | MODIFIER | c.-628G>A| |
S247 |
| 129663 | BAA10g17500 | A10 | 16813857 | C | T | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S156 |
| 129664 | BAA10g17510 | A10 | 16814744 | C | T | stop_gained | HIGH | c.1488G>A|p.Trp496* |
S271 |
| 129665 | BAA10g17510 | A10 | 16814893 | G | A | synonymous_variant | LOW | c.1339C>T|p.Leu447Leu |
S43 |
| 129666 | BAA10g17510 | A10 | 16815144 | G | A | missense_variant | MODERATE | c.1088C>T|p.Pro363Leu |
S112 |
| 129667 | BAA10g17510 | A10 | 16815159 | C | T | missense_variant | MODERATE | c.1073G>A|p.Gly358Asp |
S123 |
| 129668 | BAA10g17510 | A10 | 16815474 | G | A | missense_variant | MODERATE | c.758C>T|p.Ser253Phe |
S53 |
| 129669 | BAA10g17510 | A10 | 16816119 | G | A | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S292 |
| 129670 | BAA10g17510 | A10 | 16818549 | G | A | upstream_gene_variant | MODIFIER | c.-2318C>T| |
S178 |
| 129671 | BAA10g17510 | A10 | 16818924 | G | A | upstream_gene_variant | MODIFIER | c.-2693C>T| |
S270 |
| 129672 | BAA10g17510 | A10 | 16819260 | G | A | upstream_gene_variant | MODIFIER | c.-3029C>T| |
S165 |
| 129673 | BAA10g17510 | A10 | 16819338 | G | A | upstream_gene_variant | MODIFIER | c.-3107C>T| |
S42 |
| 129674 | BAA10g17510 | A10 | 16819661 | C | T | upstream_gene_variant | MODIFIER | c.-3430G>A| |
S296 |
| 129675 | BAA10g17510 | A10 | 16819960 | G | A | upstream_gene_variant | MODIFIER | c.-3729C>T| |
S1 S90 |