Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46670 | A01 | 31063299 | G | A | synonymous_variant | LOW | c.432G>A|p.Gln144Gln |
S233 |
2 | BAA01g46670 | A01 | 31063880 | G | A | synonymous_variant | LOW | c.738G>A|p.Glu246Glu |
S241 |
3 | BAA01g46670 | A01 | 31064374 | C | T | synonymous_variant | LOW | c.1137C>T|p.Ser379Ser |
S299 |
4 | BAA01g46670 | A01 | 31064765 | C | T | missense_variant | MODERATE | c.1421C>T|p.Ser474Phe |
S5 |
5 | BAA01g46670 | A01 | 31064980 | G | A | missense_variant | MODERATE | c.1636G>A|p.Val546Met |
S279 |
6 | BAA01g46670 | A01 | 31065001 | G | A | missense_variant | MODERATE | c.1657G>A|p.Glu553Lys |
S273 |
7 | BAA01g46670 | A01 | 31065275 | G | A | missense_variant | MODERATE | c.1931G>A|p.Arg644Lys |
S39 |
8 | BAA01g46670 | A01 | 31065596 | C | T | missense_variant | MODERATE | c.2252C>T|p.Pro751Leu |
S173 |
9 | BAA01g46670 | A01 | 31065762 | G | A | missense_variant&splice_region_variant | MODERATE | c.2335G>A|p.Gly779Arg |
S277 |
10 | BAA01g46670 | A01 | 31066070 | C | T | splice_region_variant&intron_variant | LOW | c.2565-5C>T| |
S245 |
11 | BAA01g46670 | A01 | 31066114 | C | T | synonymous_variant | LOW | c.2604C>T|p.Ile868Ile |
S95 |
12 | BAA01g46670 | A01 | 31066173 | C | T | missense_variant | MODERATE | c.2663C>T|p.Ser888Phe |
|
13 | BAA01g46670 | A01 | 31067065 | G | A | missense_variant | MODERATE | c.3112G>A|p.Glu1038Lys |
S130 |