| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158851 | BAA02g06380 | A02 | 2710166 | G | A | upstream_gene_variant | MODIFIER | c.-2732C>T| |
S84 S93 |
| 158852 | BAA02g06390 | A02 | 2710803 | G | A | splice_region_variant&intron_variant | LOW | c.139+5G>A| |
S53 |
| 158853 | BAA02g06390 | A02 | 2711761 | C | T | missense_variant | MODERATE | c.331C>T|p.Leu111Phe |
S15 S3 |
| 158854 | BAA02g06380 | A02 | 2712164 | G | A | upstream_gene_variant | MODIFIER | c.-4730C>T| |
S140 |
| 158855 | BAA02g06400 | A02 | 2714071 | G | A | upstream_gene_variant | MODIFIER | c.-503G>A| |
S161 |
| 158856 | BAA02g06400 | A02 | 2714101 | A | G | upstream_gene_variant | MODIFIER | c.-473A>G| |
S251 |
| 158857 | BAA02g06400 | A02 | 2714554 | G | A | upstream_gene_variant | MODIFIER | c.-20G>A| |
S305 |
| 158858 | BAA02g06410 | A02 | 2715059 | C | T | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S19 |
| 158859 | BAA02g06410 | A02 | 2715306 | G | A | upstream_gene_variant | MODIFIER | c.-2690G>A| |
S156 |
| 158860 | BAA02g06400 | A02 | 2716706 | C | T | synonymous_variant | LOW | c.831C>T|p.Gly277Gly |
S306 S308 |
| 158861 | BAA02g06400 | A02 | 2716800 | G | A | missense_variant | MODERATE | c.925G>A|p.Val309Met |
S165 |
| 158862 | BAA02g06400 | A02 | 2716806 | C | T | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S298 |
| 158863 | BAA02g06400 | A02 | 2717136 | G | A | missense_variant | MODERATE | c.1261G>A|p.Asp421Asn |
S17 |
| 158864 | BAA02g06410 | A02 | 2717871 | G | A | upstream_gene_variant | MODIFIER | c.-125G>A| |
S261 S303 |
| 158865 | BAA02g06410 | A02 | 2718265 | C | T | synonymous_variant | LOW | c.270C>T|p.Phe90Phe |
S111 |
| 158866 | BAA02g06410 | A02 | 2718315 | C | T | missense_variant | MODERATE | c.320C>T|p.Ser107Phe |
S179 |
| 158867 | BAA02g06410 | A02 | 2719144 | G | A | synonymous_variant | LOW | c.1149G>A|p.Gly383Gly |
S156 |
| 158868 | BAA02g06410 | A02 | 2719201 | G | A | synonymous_variant | LOW | c.1206G>A|p.Glu402Glu |
S67 |
| 158869 | BAA02g06410 | A02 | 2719323 | G | A | missense_variant | MODERATE | c.1328G>A|p.Ser443Asn |
S89 |
| 158870 | BAA02g06410 | A02 | 2719587 | C | T | missense_variant | MODERATE | c.1592C>T|p.Ser531Phe |
S115 |
| 158871 | BAA02g06410 | A02 | 2719621 | C | T | synonymous_variant | LOW | c.1626C>T|p.Leu542Leu |
S64 |
| 158872 | BAA02g06410 | A02 | 2720219 | G | A | missense_variant | MODERATE | c.2224G>A|p.Asp742Asn |
S282 |
| 158873 | BAA02g06410 | A02 | 2720470 | G | A | synonymous_variant | LOW | c.2475G>A|p.Lys825Lys |
S155 |
| 158874 | BAA02g06410 | A02 | 2720712 | C | T | missense_variant | MODERATE | c.2717C>T|p.Ser906Phe |
S37 |
| 158875 | BAA02g06410 | A02 | 2720734 | G | A | synonymous_variant | LOW | c.2739G>A|p.Lys913Lys |
S241 |