| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 149651 | BAA10g33710 | A10 | 23935186 | C | T | upstream_gene_variant | MODIFIER | c.-3234G>A| |
S201 |
| 149652 | BAA10g33720 | A10 | 23936549 | G | A | synonymous_variant | LOW | c.285G>A|p.Thr95Thr |
S263 |
| 149653 | BAA10g33720 | A10 | 23937562 | G | A | downstream_gene_variant | MODIFIER | c.*505G>A| |
S1 S90 |
| 149654 | BAA10g33730 | A10 | 23938887 | C | T | upstream_gene_variant | MODIFIER | c.-403G>A| |
S142 |
| 149655 | BAA10g33730 | A10 | 23938994 | A | G | upstream_gene_variant | MODIFIER | c.-510T>C| |
S257 |
| 149656 | BAA10g33730 | A10 | 23939478 | G | A | upstream_gene_variant | MODIFIER | c.-994C>T| |
S138 |
| 149657 | BAA10g33730 | A10 | 23939500 | C | T | upstream_gene_variant | MODIFIER | c.-1016G>A| |
S98 |
| 149658 | BAA10g33730 | A10 | 23940036 | G | A | upstream_gene_variant | MODIFIER | c.-1552C>T| |
S35 |
| 149659 | BAA10g33730 | A10 | 23940384 | C | T | upstream_gene_variant | MODIFIER | c.-1900G>A| |
S18 |
| 149660 | BAA10g33730 | A10 | 23941256 | C | T | upstream_gene_variant | MODIFIER | c.-2772G>A| |
S2 |
| 149661 | BAA10g33730 | A10 | 23941917 | C | T | upstream_gene_variant | MODIFIER | c.-3433G>A| |
S6 |
| 149662 | BAA10g33730 | A10 | 23942087 | A | T | upstream_gene_variant | MODIFIER | c.-3603T>A| |
S153 |
| 149663 | BAA10g33730 | A10 | 23942944 | C | T | upstream_gene_variant | MODIFIER | c.-4460G>A| |
S36 |
| 149664 | BAA10g33730 | A10 | 23942965 | G | A | upstream_gene_variant | MODIFIER | c.-4481C>T| |
S71 |
| 149665 | BAA10g33740 | A10 | 23944062 | C | T | upstream_gene_variant | MODIFIER | c.-1520G>A| |
S86 |
| 149666 | BAA10g33740 | A10 | 23945800 | G | A | upstream_gene_variant | MODIFIER | c.-3258C>T| |
S130 |
| 149667 | BAA10g33740 | A10 | 23946532 | C | T | upstream_gene_variant | MODIFIER | c.-3990G>A| |
S33 |
| 149668 | BAA10g33740 | A10 | 23947504 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S295 |
| 149669 | BAA10g33770 | A10 | 23947873 | C | T | missense_variant | MODERATE | c.229C>T|p.Pro77Ser |
S87 |
| 149670 | BAA10g33770 | A10 | 23948118 | C | T | synonymous_variant | LOW | c.390C>T|p.Ile130Ile |
S40 S49 |
| 149671 | BAA10g33770 | A10 | 23948920 | C | T | missense_variant&splice_region_variant | MODERATE | c.797C>T|p.Ser266Phe |
S152 |
| 149672 | BAA10g33770 | A10 | 23949317 | C | T | synonymous_variant | LOW | c.1020C>T|p.Arg340Arg |
S232 |
| 149673 | BAA10g33760 | A10 | 23950058 | C | T | downstream_gene_variant | MODIFIER | c.*3912C>T| |
S295 |
| 149674 | BAA10g33760 | A10 | 23950847 | C | T | downstream_gene_variant | MODIFIER | c.*4701C>T| |
S194 |
| 149675 | BAA10g33780 | A10 | 23953585 | C | T | synonymous_variant | LOW | c.114G>A|p.Gln38Gln |
S13 |