| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g15090 | A01 | 7191184 | G | A | upstream_gene_variant | MODIFIER | c.-4933G>A| |
S175 |
| 2 | BAA01g15090 | A01 | 7191254 | C | T | upstream_gene_variant | MODIFIER | c.-4863C>T| |
S112 |
| 3 | BAA01g15090 | A01 | 7191738 | C | T | upstream_gene_variant | MODIFIER | c.-4379C>T| |
S11 |
| 4 | BAA01g15090 | A01 | 7192218 | G | A | upstream_gene_variant | MODIFIER | c.-3899G>A| |
S37 |
| 5 | BAA01g15090 | A01 | 7194934 | G | A | upstream_gene_variant | MODIFIER | c.-1183G>A| |
S168 |
| 6 | BAA01g15090 | A01 | 7194946 | G | A | upstream_gene_variant | MODIFIER | c.-1171G>A| |
S287 |
| 7 | BAA01g15090 | A01 | 7195215 | G | A | upstream_gene_variant | MODIFIER | c.-902G>A| |
S294 |
| 8 | BAA01g15090 | A01 | 7195437 | G | A | upstream_gene_variant | MODIFIER | c.-680G>A| |
S195 |
| 9 | BAA01g15090 | A01 | 7196389 | G | A | missense_variant | MODERATE | c.182G>A|p.Arg61His |
S97 |
| 10 | BAA01g15090 | A01 | 7196403 | G | A | missense_variant | MODERATE | c.196G>A|p.Glu66Lys |
S104 S52 |
| 11 | BAA01g15090 | A01 | 7196503 | C | T | missense_variant | MODERATE | c.296C>T|p.Ser99Phe |
S164 |
| 12 | BAA01g15090 | A01 | 7196542 | G | A | missense_variant | MODERATE | c.335G>A|p.Gly112Glu |
S28 |
| 13 | BAA01g15090 | A01 | 7197774 | G | A | splice_region_variant&intron_variant | LOW | c.1099+3G>A| |
S175 |
| 14 | BAA01g15090 | A01 | 7198625 | C | T | missense_variant | MODERATE | c.1295C>T|p.Ser432Phe |
S200 |
| 15 | BAA01g15090 | A01 | 7198701 | G | A | synonymous_variant | LOW | c.1371G>A|p.Arg457Arg |
S23 |
| 16 | BAA01g15090 | A01 | 7202175 | C | T | missense_variant | MODERATE | c.2269C>T|p.Arg757Trp |
S242 |
| 17 | BAA01g15090 | A01 | 7202866 | G | A | missense_variant | MODERATE | c.2833G>A|p.Glu945Lys |
S13 |
| 18 | BAA01g15090 | A01 | 7204641 | G | A | missense_variant | MODERATE | c.3085G>A|p.Asp1029Asn |
S37 |
| 19 | BAA01g15090 | A01 | 7205899 | C | T | downstream_gene_variant | MODIFIER | c.*1187C>T| |
S46 |