| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 82751 | BAA01g43960 | A01 | 29093870 | G | A | missense_variant | MODERATE | c.895G>A|p.Ala299Thr |
S252 |
| 82752 | BAA01g43960 | A01 | 29093893 | G | A | synonymous_variant | LOW | c.918G>A|p.Lys306Lys |
S98 |
| 82753 | BAA01g43960 | A01 | 29094047 | G | A | missense_variant | MODERATE | c.995G>A|p.Gly332Glu |
S149 |
| 82754 | BAA01g43950 | A01 | 29094486 | G | A | upstream_gene_variant | MODIFIER | c.-2819C>T| |
S175 |
| 82755 | BAA01g43950 | A01 | 29096151 | C | T | upstream_gene_variant | MODIFIER | c.-4484G>A| |
S302 |
| 82756 | BAA01g43960 | A01 | 29096190 | C | T | synonymous_variant | LOW | c.1998C>T|p.Tyr666Tyr |
S305 |
| 82757 | BAA01g43950 | A01 | 29096313 | G | A | upstream_gene_variant | MODIFIER | c.-4646C>T| |
S139 |
| 82758 | BAA01g43960 | A01 | 29096941 | C | T | missense_variant | MODERATE | c.2224C>T|p.Arg742Cys |
S46 |
| 82759 | BAA01g43960 | A01 | 29097379 | C | T | intron_variant | MODIFIER | c.2344-10C>T| |
S58 |
| 82760 | BAA01g43960 | A01 | 29098115 | G | A | missense_variant | MODERATE | c.2792G>A|p.Gly931Glu |
S243 S299 |
| 82761 | BAA01g43960 | A01 | 29098461 | C | T | missense_variant | MODERATE | c.2902C>T|p.His968Tyr |
S279 |
| 82762 | BAA01g43960 | A01 | 29099234 | C | T | missense_variant | MODERATE | c.3349C>T|p.Leu1117Phe |
S97 |
| 82763 | BAA01g43970 | A01 | 29100823 | C | T | downstream_gene_variant | MODIFIER | c.*3012G>A| |
S182 |
| 82764 | BAA01g43970 | A01 | 29105445 | C | T | missense_variant&splice_region_variant | MODERATE | c.1546G>A|p.Glu516Lys |
S182 |
| 82765 | BAA01g43970 | A01 | 29105579 | G | A | missense_variant | MODERATE | c.1483C>T|p.His495Tyr |
S232 |
| 82766 | BAA01g43970 | A01 | 29106304 | C | T | splice_region_variant&intron_variant | LOW | c.1460+4G>A| |
S301 S304 |
| 82767 | BAA01g43970 | A01 | 29106411 | G | A | synonymous_variant | LOW | c.1357C>T|p.Leu453Leu |
S122 |
| 82768 | BAA01g43970 | A01 | 29107089 | G | A | stop_gained | HIGH | c.679C>T|p.Arg227* |
S117 |
| 82769 | BAA01g43970 | A01 | 29107109 | C | T | missense_variant | MODERATE | c.659G>A|p.Gly220Glu |
S240 |
| 82770 | BAA01g43970 | A01 | 29107692 | C | T | missense_variant | MODERATE | c.76G>A|p.Glu26Lys |
S68 |
| 82771 | BAA01g43970 | A01 | 29108015 | C | T | upstream_gene_variant | MODIFIER | c.-248G>A| |
S275 |
| 82772 | BAA01g43970 | A01 | 29108078 | G | A | upstream_gene_variant | MODIFIER | c.-311C>T| |
S241 |
| 82773 | BAA01g43970 | A01 | 29108424 | C | T | upstream_gene_variant | MODIFIER | c.-657G>A| |
S44 |
| 82774 | BAA01g43970 | A01 | 29109085 | C | T | upstream_gene_variant | MODIFIER | c.-1318G>A| |
S294 |
| 82775 | BAA01g43980 | A01 | 29110504 | C | T | synonymous_variant | LOW | c.546C>T|p.His182His |
S157 |