| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 136801 | BAA10g22480 | A10 | 19296239 | G | A | upstream_gene_variant | MODIFIER | c.-121C>T| |
S16 |
| 136802 | BAA10g22480 | A10 | 19296709 | G | A | upstream_gene_variant | MODIFIER | c.-591C>T| |
S284 |
| 136803 | BAA10g22480 | A10 | 19297189 | C | T | upstream_gene_variant | MODIFIER | c.-1071G>A| |
S33 |
| 136804 | BAA10g22480 | A10 | 19297772 | C | T | upstream_gene_variant | MODIFIER | c.-1654G>A| |
S297 |
| 136805 | BAA10g22480 | A10 | 19298250 | G | A | upstream_gene_variant | MODIFIER | c.-2132C>T| |
S62 |
| 136806 | BAA10g22490 | A10 | 19298861 | C | T | synonymous_variant | LOW | c.264C>T|p.Phe88Phe |
S51 |
| 136807 | BAA10g22490 | A10 | 19298864 | C | T | synonymous_variant | LOW | c.267C>T|p.Phe89Phe |
S221 |
| 136808 | BAA10g22490 | A10 | 19299113 | C | T | synonymous_variant | LOW | c.516C>T|p.Asn172Asn |
S23 |
| 136809 | BAA10g22490 | A10 | 19299115 | C | T | missense_variant | MODERATE | c.518C>T|p.Ser173Phe |
S148 S210 S30 S31 |
| 136810 | BAA10g22480 | A10 | 19300358 | G | A | upstream_gene_variant | MODIFIER | c.-4240C>T| |
S294 |
| 136811 | BAA10g22480 | A10 | 19300533 | C | T | upstream_gene_variant | MODIFIER | c.-4415G>A| |
S206 S26 |
| 136812 | BAA10g22490 | A10 | 19301151 | C | T | downstream_gene_variant | MODIFIER | c.*826C>T| |
S146 |
| 136813 | BAA10g22500 | A10 | 19301583 | C | T | upstream_gene_variant | MODIFIER | c.-16G>A| |
S38 |
| 136814 | BAA10g22500 | A10 | 19302210 | C | T | upstream_gene_variant | MODIFIER | c.-643G>A| |
S144 |
| 136815 | BAA10g22510 | A10 | 19302835 | C | T | missense_variant | MODERATE | c.1345G>A|p.Ala449Thr |
S34 |
| 136816 | BAA10g22510 | A10 | 19303188 | G | A | missense_variant | MODERATE | c.992C>T|p.Ser331Leu |
S61 |
| 136817 | BAA10g22510 | A10 | 19303266 | G | A | missense_variant | MODERATE | c.914C>T|p.Thr305Ile |
S18 |
| 136818 | BAA10g22510 | A10 | 19303594 | C | T | missense_variant | MODERATE | c.586G>A|p.Asp196Asn |
S150 |
| 136819 | BAA10g22510 | A10 | 19303781 | G | A | synonymous_variant | LOW | c.399C>T|p.Leu133Leu |
S191 |
| 136820 | BAA10g22510 | A10 | 19303856 | G | A | synonymous_variant | LOW | c.324C>T|p.Phe108Phe |
S219 S72 |
| 136821 | BAA10g22510 | A10 | 19303878 | C | T | missense_variant | MODERATE | c.302G>A|p.Gly101Asp |
S275 |
| 136822 | BAA10g22500 | A10 | 19304271 | G | A | upstream_gene_variant | MODIFIER | c.-2704C>T| |
S35 |
| 136823 | BAA10g22500 | A10 | 19304288 | G | A | upstream_gene_variant | MODIFIER | c.-2721C>T| |
S61 |
| 136824 | BAA10g22500 | A10 | 19304838 | C | T | upstream_gene_variant | MODIFIER | c.-3271G>A| |
S291 |
| 136825 | BAA10g22500 | A10 | 19305064 | G | A | upstream_gene_variant | MODIFIER | c.-3497C>T| |
S208 |