| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g19940 | A07 | 25397901 | G | A | upstream_gene_variant | MODIFIER | c.-4959G>A| |
S11 |
| 2 | BAA07g19940 | A07 | 25398843 | C | T | upstream_gene_variant | MODIFIER | c.-4017C>T| |
S293 |
| 3 | BAA07g19940 | A07 | 25404050 | C | T | missense_variant | MODERATE | c.653C>T|p.Pro218Leu |
S203 |
| 4 | BAA07g19940 | A07 | 25404051 | G | A | synonymous_variant | LOW | c.654G>A|p.Pro218Pro |
S74 |
| 5 | BAA07g19940 | A07 | 25404064 | T | A | missense_variant | MODERATE | c.667T>A|p.Tyr223Asn |
S148 S210 S30 |
| 6 | BAA07g19940 | A07 | 25404398 | C | T | synonymous_variant | LOW | c.831C>T|p.Phe277Phe |
S303 |
| 7 | BAA07g19940 | A07 | 25404842 | C | T | missense_variant | MODERATE | c.1204C>T|p.Pro402Ser |
S99 |
| 8 | BAA07g19940 | A07 | 25404857 | C | T | missense_variant | MODERATE | c.1219C>T|p.Leu407Phe |
S19 |
| 9 | BAA07g19940 | A07 | 25406418 | C | T | downstream_gene_variant | MODIFIER | c.*616C>T| |
S255 |
| 10 | BAA07g19940 | A07 | 25408377 | G | A | downstream_gene_variant | MODIFIER | c.*2575G>A| |
S188 |