Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68730 | A09 | 61671784 | G | A | synonymous_variant | LOW | c.162G>A|p.Arg54Arg |
S45 |
2 | BAA09g68730 | A09 | 61672738 | G | A | synonymous_variant | LOW | c.1116G>A|p.Glu372Glu |
S209 |
3 | BAA09g68730 | A09 | 61672934 | G | A | missense_variant | MODERATE | c.1312G>A|p.Asp438Asn |
S161 |
4 | BAA09g68730 | A09 | 61673086 | G | A | synonymous_variant | LOW | c.1464G>A|p.Leu488Leu |
S284 |
5 | BAA09g68730 | A09 | 61673152 | G | A | synonymous_variant | LOW | c.1530G>A|p.Gln510Gln |
S297 |
6 | BAA09g68730 | A09 | 61674009 | G | A | missense_variant | MODERATE | c.2387G>A|p.Arg796His |
S113 |
7 | BAA09g68730 | A09 | 61674530 | G | A | missense_variant | MODERATE | c.2908G>A|p.Val970Ile |
S195 |
8 | BAA09g68730 | A09 | 61674653 | G | A | missense_variant | MODERATE | c.3031G>A|p.Asp1011Asn |
S42 |
9 | BAA09g68730 | A09 | 61674676 | G | A | synonymous_variant | LOW | c.3054G>A|p.Glu1018Glu |
S152 S185 S273 S68 |
10 | BAA09g68730 | A09 | 61675226 | G | A | missense_variant | MODERATE | c.3604G>A|p.Glu1202Lys |
S221 |
11 | BAA09g68730 | A09 | 61675447 | G | A | intron_variant | MODIFIER | c.3736-42G>A| |
S25 |
12 | BAA09g68730 | A09 | 61675573 | G | A | missense_variant | MODERATE | c.3820G>A|p.Val1274Ile |
S298 |