| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 138951 | BAA10g24340 | A10 | 20091327 | C | T | upstream_gene_variant | MODIFIER | c.-3648G>A| |
S97 |
| 138952 | BAA10g24350 | A10 | 20092873 | C | T | downstream_gene_variant | MODIFIER | c.*179G>A| |
S108 |
| 138953 | BAA10g24350 | A10 | 20092937 | C | T | downstream_gene_variant | MODIFIER | c.*115G>A| |
S286 |
| 138954 | BAA10g24370 | A10 | 20093974 | G | A | upstream_gene_variant | MODIFIER | c.-4490G>A| |
S61 |
| 138955 | BAA10g24350 | A10 | 20094424 | C | T | missense_variant | MODERATE | c.509G>A|p.Gly170Asp |
S10 |
| 138956 | BAA10g24370 | A10 | 20094823 | G | A | upstream_gene_variant | MODIFIER | c.-3641G>A| |
S226 |
| 138957 | BAA10g24350 | A10 | 20096648 | A | C | upstream_gene_variant | MODIFIER | c.-1560T>G| |
S217 |
| 138958 | BAA10g24360 | A10 | 20097016 | C | T | missense_variant | MODERATE | c.4G>A|p.Gly2Arg |
S86 |
| 138959 | BAA10g24350 | A10 | 20097329 | C | T | upstream_gene_variant | MODIFIER | c.-2241G>A| |
S183 |
| 138960 | BAA10g24350 | A10 | 20097658 | G | A | upstream_gene_variant | MODIFIER | c.-2570C>T| |
S293 |
| 138961 | BAA10g24350 | A10 | 20097827 | C | T | upstream_gene_variant | MODIFIER | c.-2739G>A| |
S56 |
| 138962 | BAA10g24370 | A10 | 20098627 | G | A | missense_variant | MODERATE | c.164G>A|p.Gly55Glu |
S127 |
| 138963 | BAA10g24380 | A10 | 20100462 | G | A | missense_variant | MODERATE | c.1807C>T|p.Arg603Cys |
S192 |
| 138964 | BAA10g24380 | A10 | 20100629 | G | A | missense_variant | MODERATE | c.1640C>T|p.Ser547Phe |
S190 |
| 138965 | BAA10g24380 | A10 | 20100765 | C | T | missense_variant | MODERATE | c.1504G>A|p.Gly502Arg |
S197 |
| 138966 | BAA10g24370 | A10 | 20103207 | C | T | downstream_gene_variant | MODIFIER | c.*3889C>T| |
S116 |
| 138967 | BAA10g24380 | A10 | 20103379 | G | A | missense_variant | MODERATE | c.706C>T|p.Pro236Ser |
S271 |
| 138968 | BAA10g24380 | A10 | 20103562 | C | T | missense_variant | MODERATE | c.523G>A|p.Asp175Asn |
S224 |
| 138969 | BAA10g24380 | A10 | 20103693 | C | T | missense_variant | MODERATE | c.392G>A|p.Gly131Asp |
S247 |
| 138970 | BAA10g24380 | A10 | 20103825 | C | T | missense_variant | MODERATE | c.260G>A|p.Cys87Tyr |
S152 |
| 138971 | BAA10g24380 | A10 | 20104795 | G | A | upstream_gene_variant | MODIFIER | c.-633C>T| |
S112 |
| 138972 | BAA10g24380 | A10 | 20105834 | C | T | upstream_gene_variant | MODIFIER | c.-1672G>A| |
S259 |
| 138973 | BAA10g24380 | A10 | 20105988 | C | T | upstream_gene_variant | MODIFIER | c.-1826G>A| |
S12 |
| 138974 | BAA10g24380 | A10 | 20106846 | C | T | upstream_gene_variant | MODIFIER | c.-2684G>A| |
S265 S39 |
| 138975 | BAA10g24380 | A10 | 20107063 | G | A | upstream_gene_variant | MODIFIER | c.-2901C>T| |
S136 |