| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g37460 | A09 | 45588668 | C | T | downstream_gene_variant | MODIFIER | c.*1195G>A| |
S36 |
| 2 | BAA09g37460 | A09 | 45588889 | G | A | downstream_gene_variant | MODIFIER | c.*974C>T| |
S289 S290 |
| 3 | BAA09g37460 | A09 | 45589862 | C | T | downstream_gene_variant | MODIFIER | c.*1G>A| |
S132 S137 S138 S237 S288 S89 |
| 4 | BAA09g37460 | A09 | 45589898 | G | A | synonymous_variant | LOW | c.1795C>T|p.Leu599Leu |
S167 |
| 5 | BAA09g37460 | A09 | 45590764 | G | A | synonymous_variant | LOW | c.1114C>T|p.Leu372Leu |
S35 |
| 6 | BAA09g37460 | A09 | 45591159 | G | A | synonymous_variant | LOW | c.795C>T|p.Ser265Ser |
S218 |
| 7 | BAA09g37460 | A09 | 45591372 | G | A | intron_variant | MODIFIER | c.700-36C>T| |
S202 |
| 8 | BAA09g37460 | A09 | 45591749 | C | T | intron_variant | MODIFIER | c.513-147G>A| |
S47 |
| 9 | BAA09g37460 | A09 | 45592277 | C | T | intron_variant | MODIFIER | c.271-35G>A| |
S146 S32 |
| 10 | BAA09g37460 | A09 | 45592580 | C | T | missense_variant | MODERATE | c.58G>A|p.Val20Met |
S188 |
| 11 | BAA09g37460 | A09 | 45593767 | C | T | upstream_gene_variant | MODIFIER | c.-1130G>A| |
S269 |
| 12 | BAA09g37460 | A09 | 45595027 | C | T | upstream_gene_variant | MODIFIER | c.-2390G>A| |
S219 S72 |
| 13 | BAA09g37460 | A09 | 45595087 | G | A | upstream_gene_variant | MODIFIER | c.-2450C>T| |
S308 |
| 14 | BAA09g37460 | A09 | 45595372 | G | A | upstream_gene_variant | MODIFIER | c.-2735C>T| |
S65 |
| 15 | BAA09g37460 | A09 | 45595600 | G | A | upstream_gene_variant | MODIFIER | c.-2963C>T| |
S12 |
| 16 | BAA09g37460 | A09 | 45596534 | C | T | upstream_gene_variant | MODIFIER | c.-3897G>A| |
S152 |
| 17 | BAA09g37460 | A09 | 45596790 | G | A | upstream_gene_variant | MODIFIER | c.-4153C>T| |
S4 |
| 18 | BAA09g37460 | A09 | 45597348 | G | A | upstream_gene_variant | MODIFIER | c.-4711C>T| |
S67 |
| 19 | BAA09g37460 | A09 | 45597399 | C | T | upstream_gene_variant | MODIFIER | c.-4762G>A| |
S210 S225 |
| 20 | BAA09g37460 | A09 | 45597447 | G | A | upstream_gene_variant | MODIFIER | c.-4810C>T| |
S265 |