| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 203551 | BAA02g31490 | A02 | 18930796 | G | A | missense_variant | MODERATE | c.268C>T|p.Arg90Trp |
S97 |
| 203552 | BAA02g31490 | A02 | 18930907 | C | T | missense_variant | MODERATE | c.157G>A|p.Ala53Thr |
S276 |
| 203553 | BAA02g31480 | A02 | 18931639 | G | A | upstream_gene_variant | MODIFIER | c.-1953C>T| |
S249 |
| 203554 | BAA02g31480 | A02 | 18931916 | C | T | upstream_gene_variant | MODIFIER | c.-2230G>A| |
S299 |
| 203555 | BAA02g31480 | A02 | 18932092 | C | T | upstream_gene_variant | MODIFIER | c.-2406G>A| |
S6 |
| 203556 | BAA02g31480 | A02 | 18932227 | G | A | upstream_gene_variant | MODIFIER | c.-2541C>T| |
S260 |
| 203557 | BAA02g31480 | A02 | 18932906 | G | A | upstream_gene_variant | MODIFIER | c.-3220C>T| |
S59 |
| 203558 | BAA02g31480 | A02 | 18933267 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S150 |
| 203559 | BAA02g31480 | A02 | 18933322 | G | A | upstream_gene_variant | MODIFIER | c.-3636C>T| |
S132 S137 S215 S89 |
| 203560 | BAA02g31500 | A02 | 18943844 | G | A | missense_variant | MODERATE | c.194G>A|p.Cys65Tyr |
S67 |
| 203561 | BAA02g31500 | A02 | 18944168 | G | A | downstream_gene_variant | MODIFIER | c.*126G>A| |
S35 |
| 203562 | BAA02g31520 | A02 | 18944996 | C | T | upstream_gene_variant | MODIFIER | c.-4838C>T| |
S112 |
| 203563 | BAA02g31510 | A02 | 18945096 | C | T | missense_variant | MODERATE | c.3109G>A|p.Glu1037Lys |
S8 |
| 203564 | BAA02g31520 | A02 | 18945531 | G | A | upstream_gene_variant | MODIFIER | c.-4303G>A| |
S207 |
| 203565 | BAA02g31510 | A02 | 18945818 | G | A | splice_region_variant&intron_variant | LOW | c.2969+6C>T| |
S45 |
| 203566 | BAA02g31510 | A02 | 18946038 | G | A | missense_variant | MODERATE | c.2755C>T|p.Pro919Ser |
S47 |
| 203567 | BAA02g31510 | A02 | 18946224 | G | A | missense_variant | MODERATE | c.2569C>T|p.Leu857Phe |
S134 |
| 203568 | BAA02g31510 | A02 | 18946788 | G | A | missense_variant | MODERATE | c.2159C>T|p.Pro720Leu |
S302 |
| 203569 | BAA02g31510 | A02 | 18946977 | G | A | missense_variant | MODERATE | c.2062C>T|p.Pro688Ser |
S174 |
| 203570 | BAA02g31510 | A02 | 18947535 | C | T | missense_variant | MODERATE | c.1504G>A|p.Val502Ile |
S131 |
| 203571 | BAA02g31510 | A02 | 18947667 | C | T | splice_region_variant&intron_variant | LOW | c.1405-4G>A| |
S182 |
| 203572 | BAA02g31510 | A02 | 18947821 | G | A | missense_variant | MODERATE | c.1333C>T|p.Pro445Ser |
S71 |
| 203573 | BAA02g31510 | A02 | 18948144 | G | A | synonymous_variant | LOW | c.1266C>T|p.Arg422Arg |
S48 |
| 203574 | BAA02g31510 | A02 | 18948160 | G | A | missense_variant | MODERATE | c.1250C>T|p.Ser417Leu |
S191 |
| 203575 | BAA02g31510 | A02 | 18948360 | G | A | synonymous_variant | LOW | c.1050C>T|p.Asp350Asp |
S249 |