| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 114551 | BAA10g09330 | A10 | 11318868 | C | T | missense_variant | MODERATE | c.1645G>A|p.Asp549Asn |
S37 |
| 114552 | BAA10g09330 | A10 | 11320389 | A | C | synonymous_variant | LOW | c.402T>G|p.Val134Val |
S130 |
| 114553 | BAA10g09330 | A10 | 11321625 | C | T | upstream_gene_variant | MODIFIER | c.-580G>A| |
S232 |
| 114554 | BAA10g09330 | A10 | 11321734 | G | A | upstream_gene_variant | MODIFIER | c.-689C>T| |
S9 |
| 114555 | BAA10g09330 | A10 | 11321738 | G | A | upstream_gene_variant | MODIFIER | c.-693C>T| |
S296 |
| 114556 | BAA10g09330 | A10 | 11321774 | C | T | upstream_gene_variant | MODIFIER | c.-729G>A| |
S225 S73 |
| 114557 | BAA10g09330 | A10 | 11321909 | C | T | upstream_gene_variant | MODIFIER | c.-864G>A| |
S5 |
| 114558 | BAA10g09330 | A10 | 11323220 | C | T | upstream_gene_variant | MODIFIER | c.-2175G>A| |
S110 S286 |
| 114559 | BAA10g09330 | A10 | 11323246 | C | T | upstream_gene_variant | MODIFIER | c.-2201G>A| |
S37 |
| 114560 | BAA10g09330 | A10 | 11324812 | C | T | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S95 |
| 114561 | BAA10g09330 | A10 | 11324919 | G | A | upstream_gene_variant | MODIFIER | c.-3874C>T| |
S212 |
| 114562 | BAA10g09330 | A10 | 11324927 | C | T | upstream_gene_variant | MODIFIER | c.-3882G>A| |
S186 |
| 114563 | BAA10g09330 | A10 | 11325098 | G | A | upstream_gene_variant | MODIFIER | c.-4053C>T| |
S112 |
| 114564 | BAA10g09340 | A10 | 11327717 | C | T | downstream_gene_variant | MODIFIER | c.*204G>A| |
S294 |
| 114565 | BAA10g09340 | A10 | 11328859 | G | A | intron_variant | MODIFIER | c.621+32C>T| |
S263 |
| 114566 | BAA10g09340 | A10 | 11328958 | G | A | missense_variant | MODERATE | c.554C>T|p.Ala185Val |
S202 |
| 114567 | BAA10g09340 | A10 | 11329261 | G | A | intron_variant | MODIFIER | c.351-100C>T| |
S295 |
| 114568 | BAA10g09340 | A10 | 11329510 | C | T | intron_variant | MODIFIER | c.351-349G>A| |
S185 |
| 114569 | BAA10g09340 | A10 | 11329635 | G | A | intron_variant | MODIFIER | c.351-474C>T| |
S172 S217 |
| 114570 | BAA10g09340 | A10 | 11329966 | G | A | intron_variant | MODIFIER | c.350+151C>T| |
S73 |
| 114571 | BAA10g09340 | A10 | 11330196 | G | A | missense_variant | MODERATE | c.271C>T|p.Pro91Ser |
S48 |
| 114572 | BAA10g09340 | A10 | 11331529 | G | A | upstream_gene_variant | MODIFIER | c.-972C>T| |
S95 |
| 114573 | BAA10g09340 | A10 | 11331845 | C | T | upstream_gene_variant | MODIFIER | c.-1288G>A| |
S297 |
| 114574 | BAA10g09340 | A10 | 11331900 | C | T | upstream_gene_variant | MODIFIER | c.-1343G>A| |
S199 |
| 114575 | BAA10g09340 | A10 | 11332475 | C | T | upstream_gene_variant | MODIFIER | c.-1918G>A| |
S206 S26 |