| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g49680 | A09 | 52912506 | T | A | downstream_gene_variant | MODIFIER | c.*1425A>T| |
S96 |
| 2 | BAA09g49680 | A09 | 52912971 | C | T | downstream_gene_variant | MODIFIER | c.*960G>A| |
S37 |
| 3 | BAA09g49680 | A09 | 52913302 | C | T | downstream_gene_variant | MODIFIER | c.*629G>A| |
S224 |
| 4 | BAA09g49680 | A09 | 52913456 | C | T | downstream_gene_variant | MODIFIER | c.*475G>A| |
S235 |
| 5 | BAA09g49680 | A09 | 52913489 | C | T | downstream_gene_variant | MODIFIER | c.*442G>A| |
S121 |
| 6 | BAA09g49680 | A09 | 52913914 | C | T | downstream_gene_variant | MODIFIER | c.*17G>A| |
S250 |
| 7 | BAA09g49680 | A09 | 52914101 | G | A | missense_variant | MODERATE | c.2008C>T|p.Leu670Phe |
S233 |
| 8 | BAA09g49680 | A09 | 52914938 | C | T | missense_variant | MODERATE | c.1517G>A|p.Gly506Glu |
S30 S31 |
| 9 | BAA09g49680 | A09 | 52915997 | G | A | missense_variant | MODERATE | c.826C>T|p.Pro276Ser |
S244 |
| 10 | BAA09g49680 | A09 | 52916852 | C | T | missense_variant | MODERATE | c.433G>A|p.Asp145Asn |
S30 S31 |
| 11 | BAA09g49680 | A09 | 52916854 | C | T | missense_variant | MODERATE | c.431G>A|p.Arg144Lys |
S87 |
| 12 | BAA09g49680 | A09 | 52918066 | C | T | upstream_gene_variant | MODIFIER | c.-299G>A| |
S256 |
| 13 | BAA09g49680 | A09 | 52918156 | G | A | upstream_gene_variant | MODIFIER | c.-389C>T| |
S171 |
| 14 | BAA09g49680 | A09 | 52918402 | C | T | upstream_gene_variant | MODIFIER | c.-635G>A| |
S210 |
| 15 | BAA09g49680 | A09 | 52918440 | C | T | upstream_gene_variant | MODIFIER | c.-673G>A| |
S275 |
| 16 | BAA09g49680 | A09 | 52918704 | C | T | upstream_gene_variant | MODIFIER | c.-937G>A| |
S18 |
| 17 | BAA09g49680 | A09 | 52919814 | C | T | upstream_gene_variant | MODIFIER | c.-2047G>A| |
S17 |
| 18 | BAA09g49680 | A09 | 52920383 | C | T | upstream_gene_variant | MODIFIER | c.-2616G>A| |
S19 |
| 19 | BAA09g49680 | A09 | 52920412 | G | A | upstream_gene_variant | MODIFIER | c.-2645C>T| |
S190 |