| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08450 | A10 | 10242625 | G | A | missense_variant | MODERATE | c.1700C>T|p.Ala567Val |
S279 |
| 2 | BAA10g08450 | A10 | 10243077 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1249-1G>A| |
S83 S88 |
| 3 | BAA10g08450 | A10 | 10243900 | G | A | synonymous_variant | LOW | c.852C>T|p.Ile284Ile |
S18 |
| 4 | BAA10g08450 | A10 | 10244195 | G | A | missense_variant | MODERATE | c.557C>T|p.Ser186Phe |
S79 S84 |
| 5 | BAA10g08450 | A10 | 10244636 | C | T | synonymous_variant | LOW | c.192G>A|p.Ala64Ala |
S42 |
| 6 | BAA10g08450 | A10 | 10247325 | G | A | upstream_gene_variant | MODIFIER | c.-2311C>T| |
S55 |
| 7 | BAA10g08450 | A10 | 10247749 | G | A | upstream_gene_variant | MODIFIER | c.-2735C>T| |
S4 |
| 8 | BAA10g08450 | A10 | 10247883 | C | T | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S44 |