Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17850 | A09 | 10735543 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1603-1G>A| |
S297 |
2 | BAA09g17850 | A09 | 10735550 | G | A | splice_region_variant&intron_variant | LOW | c.1603-8C>T| |
S172 S217 |
3 | BAA09g17850 | A09 | 10735826 | C | T | missense_variant | MODERATE | c.1507G>A|p.Ala503Thr |
S107 |
4 | BAA09g17850 | A09 | 10735973 | G | A | missense_variant | MODERATE | c.1360C>T|p.Pro454Ser |
S202 |
5 | BAA09g17850 | A09 | 10736902 | C | T | missense_variant | MODERATE | c.811G>A|p.Val271Met |
S158 |
6 | BAA09g17850 | A09 | 10736974 | C | T | missense_variant | MODERATE | c.739G>A|p.Glu247Lys |
S280 |
7 | BAA09g17850 | A09 | 10737411 | G | A | missense_variant | MODERATE | c.401C>T|p.Ala134Val |
S198 |
8 | BAA09g17850 | A09 | 10738160 | C | T | upstream_gene_variant | MODIFIER | c.-349G>A| |
S111 |
9 | BAA09g17850 | A09 | 10738205 | C | T | upstream_gene_variant | MODIFIER | c.-394G>A| |
S234 |
10 | BAA09g17850 | A09 | 10738841 | G | A | upstream_gene_variant | MODIFIER | c.-1030C>T| |
S178 |
11 | BAA09g17850 | A09 | 10739441 | G | A | upstream_gene_variant | MODIFIER | c.-1630C>T| |
S20 |
12 | BAA09g17850 | A09 | 10739811 | C | T | upstream_gene_variant | MODIFIER | c.-2000G>A| |
S213 |
13 | BAA09g17850 | A09 | 10740077 | G | A | upstream_gene_variant | MODIFIER | c.-2266C>T| |
S79 S84 |
14 | BAA09g17850 | A09 | 10740201 | G | A | upstream_gene_variant | MODIFIER | c.-2390C>T| |
S59 |
15 | BAA09g17850 | A09 | 10740749 | C | T | upstream_gene_variant | MODIFIER | c.-2938G>A| |
S128 |