| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 52701 | BAA01g29120 | A01 | 18338120 | C | T | intron_variant | MODIFIER | c.1336-82C>T| |
S134 |
| 52702 | BAA01g29120 | A01 | 18338173 | C | T | intron_variant | MODIFIER | c.1336-29C>T| |
S242 |
| 52703 | BAA01g29120 | A01 | 18339980 | C | T | synonymous_variant | LOW | c.2481C>T|p.Ile827Ile |
S219 S72 |
| 52704 | BAA01g29120 | A01 | 18340041 | G | A | missense_variant | MODERATE | c.2542G>A|p.Asp848Asn |
S246 |
| 52705 | BAA01g29120 | A01 | 18340653 | G | A | intron_variant | MODIFIER | c.2936+97G>A| |
S100 |
| 52706 | BAA01g29120 | A01 | 18341051 | C | T | intron_variant | MODIFIER | c.2937-262C>T| |
S120 |
| 52707 | BAA01g29120 | A01 | 18341142 | G | A | intron_variant | MODIFIER | c.2937-171G>A| |
S161 |
| 52708 | BAA01g29120 | A01 | 18341354 | G | A | missense_variant | MODERATE | c.2978G>A|p.Gly993Glu |
S281 |
| 52709 | BAA01g29120 | A01 | 18342418 | T | G | missense_variant | MODERATE | c.3750T>G|p.Asp1250Glu |
S105 S108 S270 |
| 52710 | BAA01g29120 | A01 | 18343022 | G | A | intron_variant | MODIFIER | c.3902+37G>A| |
S176 |
| 52711 | BAA01g29120 | A01 | 18343478 | G | A | synonymous_variant | LOW | c.3984G>A|p.Leu1328Leu |
S187 |
| 52712 | BAA01g29120 | A01 | 18343564 | G | A | missense_variant | MODERATE | c.4070G>A|p.Arg1357Lys |
S87 |
| 52713 | BAA01g29120 | A01 | 18343700 | G | A | synonymous_variant | LOW | c.4206G>A|p.Glu1402Glu |
S263 |
| 52714 | BAA01g29120 | A01 | 18343916 | T | G | missense_variant | MODERATE | c.4422T>G|p.His1474Gln |
S164 |
| 52715 | BAA01g29120 | A01 | 18344737 | C | T | missense_variant | MODERATE | c.5243C>T|p.Ser1748Phe |
S240 |
| 52716 | BAA01g29120 | A01 | 18344835 | C | T | splice_region_variant&intron_variant | LOW | c.5269-5C>T| |
S170 |
| 52717 | BAA01g29120 | A01 | 18345564 | C | T | missense_variant | MODERATE | c.5911C>T|p.Pro1971Ser |
S80 |
| 52718 | BAA01g29120 | A01 | 18345839 | C | T | intron_variant | MODIFIER | c.6074+27C>T| |
S142 |
| 52719 | BAA01g29120 | A01 | 18346489 | G | A | intron_variant | MODIFIER | c.6376-152G>A| |
S121 |
| 52720 | BAA01g29120 | A01 | 18346503 | C | T | intron_variant | MODIFIER | c.6376-138C>T| |
S279 |
| 52721 | BAA01g29120 | A01 | 18347346 | C | T | intron_variant | MODIFIER | c.6874-12C>T| |
S132 S137 S215 S284 S89 |
| 52722 | BAA01g29120 | A01 | 18348122 | G | A | missense_variant | MODERATE | c.7385G>A|p.Arg2462Lys |
S265 |
| 52723 | BAA01g29120 | A01 | 18349331 | G | A | downstream_gene_variant | MODIFIER | c.*806G>A| |
S36 |
| 52724 | BAA01g29120 | A01 | 18349546 | C | T | downstream_gene_variant | MODIFIER | c.*1021C>T| |
S273 |
| 52725 | BAA01g29120 | A01 | 18349886 | C | T | downstream_gene_variant | MODIFIER | c.*1361C>T| |
S233 |