| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 80851 | BAA01g42720 | A01 | 28312673 | C | T | missense_variant | MODERATE | c.343G>A|p.Asp115Asn |
S120 |
| 80852 | BAA01g42710 | A01 | 28313233 | G | A | upstream_gene_variant | MODIFIER | c.-4309C>T| |
S151 S263 |
| 80853 | BAA01g42710 | A01 | 28313384 | G | A | upstream_gene_variant | MODIFIER | c.-4460C>T| |
S84 S93 |
| 80854 | BAA01g42710 | A01 | 28313753 | C | T | upstream_gene_variant | MODIFIER | c.-4829G>A| |
S9 |
| 80855 | BAA01g42730 | A01 | 28314710 | G | A | synonymous_variant | LOW | c.363G>A|p.Glu121Glu |
S9 |
| 80856 | BAA01g42730 | A01 | 28314713 | C | T | synonymous_variant | LOW | c.366C>T|p.Asn122Asn |
S4 |
| 80857 | BAA01g42730 | A01 | 28314917 | C | T | missense_variant | MODERATE | c.473C>T|p.Ala158Val |
S192 |
| 80858 | BAA01g42720 | A01 | 28316527 | G | A | upstream_gene_variant | MODIFIER | c.-3009C>T| |
S196 |
| 80859 | BAA01g42720 | A01 | 28316957 | C | T | upstream_gene_variant | MODIFIER | c.-3439G>A| |
S133 |
| 80860 | BAA01g42720 | A01 | 28317019 | C | T | upstream_gene_variant | MODIFIER | c.-3501G>A| |
S59 |
| 80861 | BAA01g42720 | A01 | 28317259 | C | T | upstream_gene_variant | MODIFIER | c.-3741G>A| |
S58 S59 |
| 80862 | BAA01g42720 | A01 | 28317522 | G | A | upstream_gene_variant | MODIFIER | c.-4004C>T| |
S47 |
| 80863 | BAA01g42720 | A01 | 28318486 | G | A | upstream_gene_variant | MODIFIER | c.-4968C>T| |
S110 |
| 80864 | BAA01g42730 | A01 | 28319020 | G | A | downstream_gene_variant | MODIFIER | c.*3899G>A| |
S257 |
| 80865 | BAA01g42730 | A01 | 28319211 | G | A | downstream_gene_variant | MODIFIER | c.*4090G>A| |
S140 |
| 80866 | BAA01g42730 | A01 | 28319364 | C | T | downstream_gene_variant | MODIFIER | c.*4243C>T| |
S135 |
| 80867 | BAA01g42740 | A01 | 28322379 | G | A | upstream_gene_variant | MODIFIER | c.-2387G>A| |
S87 |
| 80868 | BAA01g42740 | A01 | 28324866 | C | T | missense_variant | MODERATE | c.101C>T|p.Pro34Leu |
S64 |
| 80869 | BAA01g42740 | A01 | 28325018 | C | T | missense_variant | MODERATE | c.253C>T|p.Pro85Ser |
S16 |
| 80870 | BAA01g42740 | A01 | 28325460 | G | A | missense_variant | MODERATE | c.619G>A|p.Glu207Lys |
S55 |
| 80871 | BAA01g42750 | A01 | 28326693 | C | T | synonymous_variant | LOW | c.714G>A|p.Arg238Arg |
S223 |
| 80872 | BAA01g42750 | A01 | 28326827 | C | T | missense_variant | MODERATE | c.664G>A|p.Asp222Asn |
S68 |
| 80873 | BAA01g42750 | A01 | 28327378 | G | A | synonymous_variant | LOW | c.345C>T|p.Ala115Ala |
S66 |
| 80874 | BAA01g42750 | A01 | 28327717 | C | T | missense_variant | MODERATE | c.202G>A|p.Ala68Thr |
S200 |
| 80875 | BAA01g42750 | A01 | 28327759 | C | T | missense_variant | MODERATE | c.160G>A|p.Ala54Thr |
S97 |