| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 118801 | BAA10g11180 | A10 | 12825330 | G | A | missense_variant | MODERATE | c.1370G>A|p.Arg457Gln |
S284 |
| 118802 | BAA10g11180 | A10 | 12825589 | C | T | missense_variant | MODERATE | c.1504C>T|p.Pro502Ser |
S149 |
| 118803 | BAA10g11190 | A10 | 12826462 | C | T | downstream_gene_variant | MODIFIER | c.*3016G>A| |
S247 |
| 118804 | BAA10g11180 | A10 | 12826760 | C | T | synonymous_variant | LOW | c.2049C>T|p.Leu683Leu |
S156 |
| 118805 | BAA10g11190 | A10 | 12827379 | C | T | downstream_gene_variant | MODIFIER | c.*2099G>A| |
S297 |
| 118806 | BAA10g11180 | A10 | 12827824 | G | A | missense_variant | MODERATE | c.2701G>A|p.Val901Ile |
S218 |
| 118807 | BAA10g11180 | A10 | 12828467 | C | T | downstream_gene_variant | MODIFIER | c.*190C>T| |
S286 |
| 118808 | BAA10g11180 | A10 | 12828941 | C | T | downstream_gene_variant | MODIFIER | c.*664C>T| |
S236 |
| 118809 | BAA10g11180 | A10 | 12828963 | G | A | downstream_gene_variant | MODIFIER | c.*686G>A| |
S4 |
| 118810 | BAA10g11180 | A10 | 12829119 | G | A | downstream_gene_variant | MODIFIER | c.*842G>A| |
S234 |
| 118811 | BAA10g11190 | A10 | 12829530 | G | A | missense_variant | MODERATE | c.665C>T|p.Ala222Val |
S18 |
| 118812 | BAA10g11190 | A10 | 12829813 | G | A | splice_region_variant&intron_variant | LOW | c.572-7C>T| |
S283 |
| 118813 | BAA10g11190 | A10 | 12830279 | T | G | missense_variant | MODERATE | c.149A>C|p.Asn50Thr |
S179 S204 S301 S303 S43 S78 |
| 118814 | BAA10g11190 | A10 | 12830339 | C | T | missense_variant | MODERATE | c.89G>A|p.Arg30Lys |
S176 |
| 118815 | BAA10g11190 | A10 | 12830551 | G | A | upstream_gene_variant | MODIFIER | c.-124C>T| |
S18 |
| 118816 | BAA10g11190 | A10 | 12831090 | G | A | upstream_gene_variant | MODIFIER | c.-663C>T| |
S262 |
| 118817 | BAA10g11190 | A10 | 12831633 | G | A | upstream_gene_variant | MODIFIER | c.-1206C>T| |
S45 |
| 118818 | BAA10g11200 | A10 | 12831728 | C | T | synonymous_variant | LOW | c.966G>A|p.Ala322Ala |
S162 |
| 118819 | BAA10g11200 | A10 | 12831924 | C | T | missense_variant | MODERATE | c.770G>A|p.Arg257His |
S152 |
| 118820 | BAA10g11200 | A10 | 12831963 | G | A | missense_variant | MODERATE | c.731C>T|p.Thr244Met |
S207 |
| 118821 | BAA10g11200 | A10 | 12832325 | G | A | synonymous_variant | LOW | c.369C>T|p.Arg123Arg |
S181 |
| 118822 | BAA10g11200 | A10 | 12832412 | C | T | synonymous_variant | LOW | c.282G>A|p.Arg94Arg |
S271 |
| 118823 | BAA10g11190 | A10 | 12833524 | C | T | upstream_gene_variant | MODIFIER | c.-3097G>A| |
S42 |
| 118824 | BAA10g11210 | A10 | 12835048 | C | T | stop_gained | HIGH | c.705G>A|p.Trp235* |
S37 |
| 118825 | BAA10g11210 | A10 | 12835203 | G | A | synonymous_variant | LOW | c.633C>T|p.Arg211Arg |
S176 |