| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 125401 | BAA10g14610 | A10 | 15252508 | G | A | downstream_gene_variant | MODIFIER | c.*3530C>T| |
S286 |
| 125402 | BAA10g14610 | A10 | 15252613 | G | A | downstream_gene_variant | MODIFIER | c.*3425C>T| |
S203 |
| 125403 | BAA10g14610 | A10 | 15254806 | G | A | downstream_gene_variant | MODIFIER | c.*1232C>T| |
S159 S243 |
| 125404 | BAA10g14610 | A10 | 15255064 | G | A | downstream_gene_variant | MODIFIER | c.*974C>T| |
S109 |
| 125405 | BAA10g14610 | A10 | 15255148 | G | A | downstream_gene_variant | MODIFIER | c.*890C>T| |
S208 |
| 125406 | BAA10g14610 | A10 | 15255224 | G | A | downstream_gene_variant | MODIFIER | c.*814C>T| |
S207 |
| 125407 | BAA10g14610 | A10 | 15255501 | C | T | downstream_gene_variant | MODIFIER | c.*537G>A| |
S156 |
| 125408 | BAA10g14610 | A10 | 15255959 | C | T | downstream_gene_variant | MODIFIER | c.*79G>A| |
S156 |
| 125409 | BAA10g14610 | A10 | 15256371 | C | T | missense_variant | MODERATE | c.162G>A|p.Met54Ile |
S256 |
| 125410 | BAA10g14610 | A10 | 15256805 | G | A | upstream_gene_variant | MODIFIER | c.-273C>T| |
S262 |
| 125411 | BAA10g14610 | A10 | 15257192 | G | A | upstream_gene_variant | MODIFIER | c.-660C>T| |
S164 |
| 125412 | BAA10g14610 | A10 | 15257515 | C | T | upstream_gene_variant | MODIFIER | c.-983G>A| |
S124 |
| 125413 | BAA10g14610 | A10 | 15257540 | C | T | upstream_gene_variant | MODIFIER | c.-1008G>A| |
S247 |
| 125414 | BAA10g14610 | A10 | 15257589 | C | T | upstream_gene_variant | MODIFIER | c.-1057G>A| |
S276 |
| 125415 | BAA10g14610 | A10 | 15258066 | C | T | upstream_gene_variant | MODIFIER | c.-1534G>A| |
S7 |
| 125416 | BAA10g14620 | A10 | 15258988 | C | T | missense_variant | MODERATE | c.2924G>A|p.Cys975Tyr |
S163 |
| 125417 | BAA10g14620 | A10 | 15260031 | C | T | synonymous_variant | LOW | c.1881G>A|p.Arg627Arg |
S247 |
| 125418 | BAA10g14620 | A10 | 15260681 | C | T | splice_region_variant&intron_variant | LOW | c.1300+5G>A| |
S225 S73 |
| 125419 | BAA10g14620 | A10 | 15261346 | G | A | missense_variant | MODERATE | c.839C>T|p.Pro280Leu |
S240 |
| 125420 | BAA10g14610 | A10 | 15261402 | C | T | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S175 |
| 125421 | BAA10g14620 | A10 | 15262477 | G | A | synonymous_variant | LOW | c.321C>T|p.Ala107Ala |
S69 |
| 125422 | BAA10g14620 | A10 | 15262649 | G | A | missense_variant | MODERATE | c.149C>T|p.Ala50Val |
S18 |
| 125423 | BAA10g14620 | A10 | 15263383 | G | A | upstream_gene_variant | MODIFIER | c.-174C>T| |
S15 |
| 125424 | BAA10g14620 | A10 | 15264073 | G | A | upstream_gene_variant | MODIFIER | c.-864C>T| |
S226 |
| 125425 | BAA10g14620 | A10 | 15265314 | C | T | upstream_gene_variant | MODIFIER | c.-2105G>A| |
S10 |