| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g19610 | A10 | 17936454 | G | A | downstream_gene_variant | MODIFIER | c.*1806C>T| |
S278 |
| 2 | BAA10g19610 | A10 | 17939353 | G | A | intron_variant | MODIFIER | c.2244-26C>T| |
S128 |
| 3 | BAA10g19610 | A10 | 17939738 | G | A | intron_variant | MODIFIER | c.1954-39C>T| |
S74 |
| 4 | BAA10g19610 | A10 | 17940313 | G | A | synonymous_variant | LOW | c.1617C>T|p.Ile539Ile |
S57 |
| 5 | BAA10g19610 | A10 | 17940938 | G | A | synonymous_variant | LOW | c.1254C>T|p.Asn418Asn |
S132 S137 S215 S89 |
| 6 | BAA10g19610 | A10 | 17941102 | C | T | synonymous_variant | LOW | c.1173G>A|p.Gln391Gln |
S156 |
| 7 | BAA10g19610 | A10 | 17941612 | C | T | intron_variant | MODIFIER | c.868-26G>A| |
S206 |
| 8 | BAA10g19610 | A10 | 17941652 | G | A | intron_variant | MODIFIER | c.867+17C>T| |
S174 |
| 9 | BAA10g19610 | A10 | 17942131 | G | A | stop_gained | HIGH | c.580C>T|p.Gln194* |
S166 |
| 10 | BAA10g19610 | A10 | 17942181 | G | A | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S35 |
| 11 | BAA10g19610 | A10 | 17942380 | C | T | missense_variant | MODERATE | c.410G>A|p.Ser137Asn |
S244 |
| 12 | BAA10g19610 | A10 | 17942434 | G | A | missense_variant | MODERATE | c.356C>T|p.Ala119Val |
S278 |
| 13 | BAA10g19610 | A10 | 17943161 | C | T | upstream_gene_variant | MODIFIER | c.-266G>A| |
S246 |
| 14 | BAA10g19610 | A10 | 17943227 | G | A | upstream_gene_variant | MODIFIER | c.-332C>T| |
S241 |
| 15 | BAA10g19610 | A10 | 17943523 | G | A | upstream_gene_variant | MODIFIER | c.-628C>T| |
S112 |
| 16 | BAA10g19610 | A10 | 17944421 | C | T | upstream_gene_variant | MODIFIER | c.-1526G>A| |
S161 |
| 17 | BAA10g19610 | A10 | 17945092 | G | A | upstream_gene_variant | MODIFIER | c.-2197C>T| |
S203 |
| 18 | BAA10g19610 | A10 | 17945439 | G | A | upstream_gene_variant | MODIFIER | c.-2544C>T| |
S111 |
| 19 | BAA10g19610 | A10 | 17946831 | C | T | upstream_gene_variant | MODIFIER | c.-3936G>A| |
S86 |
| 20 | BAA10g19610 | A10 | 17947464 | C | T | upstream_gene_variant | MODIFIER | c.-4569G>A| |
S115 |