Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14880 | A01 | 7050842 | C | T | splice_region_variant&intron_variant | LOW | c.1167+8G>A| |
S302 |
2 | BAA01g14880 | A01 | 7050849 | C | T | splice_donor_variant&intron_variant | HIGH | c.1167+1G>A| |
S155 S211 |
3 | BAA01g14880 | A01 | 7051899 | C | T | missense_variant | MODERATE | c.331G>A|p.Glu111Lys |
S270 |
4 | BAA01g14880 | A01 | 7051909 | G | A | synonymous_variant | LOW | c.321C>T|p.Phe107Phe |
S306 S308 |
5 | BAA01g14880 | A01 | 7051937 | C | T | missense_variant | MODERATE | c.293G>A|p.Gly98Asp |
S167 |
6 | BAA01g14880 | A01 | 7052348 | G | A | upstream_gene_variant | MODIFIER | c.-119C>T| |
S262 |
7 | BAA01g14880 | A01 | 7052698 | C | T | upstream_gene_variant | MODIFIER | c.-469G>A| |
S303 |
8 | BAA01g14880 | A01 | 7052947 | C | T | upstream_gene_variant | MODIFIER | c.-718G>A| |
S44 |
9 | BAA01g14880 | A01 | 7053232 | G | A | upstream_gene_variant | MODIFIER | c.-1003C>T| |
S180 |
10 | BAA01g14880 | A01 | 7053773 | C | T | upstream_gene_variant | MODIFIER | c.-1544G>A| |
S39 |
11 | BAA01g14880 | A01 | 7057168 | G | A | upstream_gene_variant | MODIFIER | c.-4939C>T| |
S284 |