| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g25690 | A10 | 20642927 | C | T | missense_variant | MODERATE | c.1127G>A|p.Gly376Asp |
S196 |
| 2 | BAA10g25690 | A10 | 20643333 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.901-1G>A| |
S51 |
| 3 | BAA10g25690 | A10 | 20645116 | G | A | missense_variant | MODERATE | c.91C>T|p.Arg31Cys |
S179 |
| 4 | BAA10g25690 | A10 | 20646327 | C | T | upstream_gene_variant | MODIFIER | c.-1121G>A| |
S250 |
| 5 | BAA10g25690 | A10 | 20647104 | C | T | upstream_gene_variant | MODIFIER | c.-1898G>A| |
S148 S210 S30 S31 |
| 6 | BAA10g25690 | A10 | 20648845 | C | T | upstream_gene_variant | MODIFIER | c.-3639G>A| |
S256 |
| 7 | BAA10g25690 | A10 | 20648898 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S282 |
| 8 | BAA10g25690 | A10 | 20648970 | C | T | upstream_gene_variant | MODIFIER | c.-3764G>A| |
S165 |
| 9 | BAA10g25690 | A10 | 20649082 | G | A | upstream_gene_variant | MODIFIER | c.-3876C>T| |
S71 |
| 10 | BAA10g25690 | A10 | 20649946 | C | T | upstream_gene_variant | MODIFIER | c.-4740G>A| |
S265 |