| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g12850 | A10 | 14172562 | G | A | upstream_gene_variant | MODIFIER | c.-4915G>A| |
S15 S3 |
| 2 | BAA10g12850 | A10 | 14173499 | C | T | upstream_gene_variant | MODIFIER | c.-3978C>T| |
S48 |
| 3 | BAA10g12850 | A10 | 14173670 | C | T | upstream_gene_variant | MODIFIER | c.-3807C>T| |
S143 |
| 4 | BAA10g12850 | A10 | 14174049 | G | A | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S61 |
| 5 | BAA10g12850 | A10 | 14175041 | G | A | upstream_gene_variant | MODIFIER | c.-2436G>A| |
S201 |
| 6 | BAA10g12850 | A10 | 14178267 | G | A | missense_variant | MODERATE | c.235G>A|p.Gly79Arg |
S65 |
| 7 | BAA10g12850 | A10 | 14178954 | G | A | splice_region_variant&intron_variant | LOW | c.637+4G>A| |
S192 |
| 8 | BAA10g12850 | A10 | 14179637 | C | T | missense_variant | MODERATE | c.1039C>T|p.Pro347Ser |
S269 |
| 9 | BAA10g12850 | A10 | 14179706 | G | A | missense_variant | MODERATE | c.1108G>A|p.Val370Ile |
S240 |
| 10 | BAA10g12850 | A10 | 14180346 | C | T | missense_variant | MODERATE | c.1289C>T|p.Pro430Leu |
S142 |
| 11 | BAA10g12850 | A10 | 14181274 | C | T | missense_variant | MODERATE | c.1630C>T|p.Leu544Phe |
S247 |
| 12 | BAA10g12850 | A10 | 14181794 | G | A | missense_variant | MODERATE | c.1933G>A|p.Asp645Asn |
S283 |
| 13 | BAA10g12850 | A10 | 14185296 | C | T | downstream_gene_variant | MODIFIER | c.*3437C>T| |
S156 |
| 14 | BAA10g12850 | A10 | 14185642 | G | A | downstream_gene_variant | MODIFIER | c.*3783G>A| |
S201 |
| 15 | BAA10g12850 | A10 | 14186349 | C | T | downstream_gene_variant | MODIFIER | c.*4490C>T| |
S37 |
| 16 | BAA10g12850 | A10 | 14186772 | T | C | downstream_gene_variant | MODIFIER | c.*4913T>C| |
S97 |