Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23570 | A09 | 14960818 | G | A | intron_variant | MODIFIER | c.48+2433G>A| |
S8 |
2 | BAA09g23570 | A09 | 14961836 | G | A | intron_variant | MODIFIER | c.49-2769G>A| |
S223 |
3 | BAA09g23570 | A09 | 14962067 | C | T | intron_variant | MODIFIER | c.49-2538C>T| |
S231 |
4 | BAA09g23570 | A09 | 14963550 | G | A | intron_variant | MODIFIER | c.49-1055G>A| |
S207 |
5 | BAA09g23570 | A09 | 14965170 | C | T | missense_variant | MODERATE | c.614C>T|p.Ala205Val |
S53 |
6 | BAA09g23570 | A09 | 14965513 | G | A | synonymous_variant | LOW | c.957G>A|p.Lys319Lys |
S201 |
7 | BAA09g23570 | A09 | 14965676 | G | A | missense_variant | MODERATE | c.1120G>A|p.Glu374Lys |
S184 |
8 | BAA09g23570 | A09 | 14965730 | C | T | missense_variant | MODERATE | c.1174C>T|p.Leu392Phe |
S64 |
9 | BAA09g23570 | A09 | 14966078 | C | T | missense_variant | MODERATE | c.1522C>T|p.Leu508Phe |
S87 |
10 | BAA09g23570 | A09 | 14966231 | C | T | intron_variant | MODIFIER | c.1548+127C>T| |
S183 |
11 | BAA09g23570 | A09 | 14967061 | G | A | intron_variant | MODIFIER | c.1549-767G>A| |
S155 S211 |
12 | BAA09g23570 | A09 | 14967355 | C | T | intron_variant | MODIFIER | c.1549-473C>T| |
S153 |
13 | BAA09g23570 | A09 | 14968829 | G | A | downstream_gene_variant | MODIFIER | c.*990G>A| |
S130 |