Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g60720 | A09 | 58188145 | C | T | missense_variant | MODERATE | c.1429G>A|p.Ala477Thr |
S174 S27 S39 |
2 | BAA09g60720 | A09 | 58188594 | C | T | missense_variant | MODERATE | c.1145G>A|p.Gly382Glu |
S156 |
3 | BAA09g60720 | A09 | 58189252 | G | A | missense_variant | MODERATE | c.734C>T|p.Ala245Val |
S178 |
4 | BAA09g60720 | A09 | 58190110 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.289-1G>A| |
S176 |
5 | BAA09g60720 | A09 | 58190618 | G | A | missense_variant | MODERATE | c.91C>T|p.Leu31Phe |
S71 |
6 | BAA09g60720 | A09 | 58190779 | C | T | upstream_gene_variant | MODIFIER | c.-71G>A| |
S153 |
7 | BAA09g60720 | A09 | 58191517 | G | A | upstream_gene_variant | MODIFIER | c.-809C>T| |
S23 |
8 | BAA09g60720 | A09 | 58191985 | C | T | upstream_gene_variant | MODIFIER | c.-1277G>A| |
S242 |
9 | BAA09g60720 | A09 | 58192668 | G | A | upstream_gene_variant | MODIFIER | c.-1960C>T| |
S193 |
10 | BAA09g60720 | A09 | 58193948 | G | A | upstream_gene_variant | MODIFIER | c.-3240C>T| |
S144 |
11 | BAA09g60720 | A09 | 58194620 | C | T | upstream_gene_variant | MODIFIER | c.-3912G>A| |
S267 |