Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21990 | A01 | 10962756 | C | T | synonymous_variant | LOW | c.225C>T|p.Val75Val |
S286 |
2 | BAA01g21990 | A01 | 10962804 | C | T | synonymous_variant | LOW | c.273C>T|p.Ser91Ser |
S91 |
3 | BAA01g21990 | A01 | 10962807 | A | C | synonymous_variant | LOW | c.276A>C|p.Ser92Ser |
S91 |
4 | BAA01g21990 | A01 | 10962816 | G | A | synonymous_variant | LOW | c.285G>A|p.Ala95Ala |
S91 |
5 | BAA01g21990 | A01 | 10962832 | G | A | missense_variant | MODERATE | c.301G>A|p.Val101Ile |
S126 |
6 | BAA01g21990 | A01 | 10962834 | T | C | synonymous_variant | LOW | c.303T>C|p.Val101Val |
S91 |
7 | BAA01g21990 | A01 | 10962837 | T | C | synonymous_variant | LOW | c.306T>C|p.Leu102Leu |
S91 |
8 | BAA01g21990 | A01 | 10962841 | C | T | missense_variant | MODERATE | c.310C>T|p.His104Tyr |
S91 |
9 | BAA01g21990 | A01 | 10962846 | T | C | synonymous_variant | LOW | c.315T>C|p.Tyr105Tyr |
S91 |
10 | BAA01g21990 | A01 | 10962857 | A | G | missense_variant | MODERATE | c.326A>G|p.Asn109Ser |
S91 |
11 | BAA01g21990 | A01 | 10962876 | C | A | synonymous_variant | LOW | c.345C>A|p.Val115Val |
S91 |
12 | BAA01g21990 | A01 | 10962888 | T | A | synonymous_variant | LOW | c.357T>A|p.Val119Val |
S91 |
13 | BAA01g21990 | A01 | 10962889 | G | T | missense_variant | MODERATE | c.358G>T|p.Val120Phe |
S91 |
14 | BAA01g21990 | A01 | 10962890 | T | C | missense_variant | MODERATE | c.359T>C|p.Val120Ala |
S91 |
15 | BAA01g21990 | A01 | 10962897 | C | G | synonymous_variant | LOW | c.366C>G|p.Ser122Ser |
S91 |
16 | BAA01g21990 | A01 | 10962905 | G | A | missense_variant | MODERATE | c.374G>A|p.Gly125Asp |
S32 |
17 | BAA01g21990 | A01 | 10962908 | G | A | missense_variant | MODERATE | c.377G>A|p.Gly126Asp |
S91 |
18 | BAA01g21990 | A01 | 10962909 | C | T | synonymous_variant | LOW | c.378C>T|p.Gly126Gly |
S91 |
19 | BAA01g21990 | A01 | 10962911 | A | T | missense_variant | MODERATE | c.380A>T|p.Asp127Val |
S91 |
20 | BAA01g21990 | A01 | 10962924 | G | C | synonymous_variant | LOW | c.393G>C|p.Ala131Ala |
S91 |
21 | BAA01g21990 | A01 | 10962957 | G | A | synonymous_variant | LOW | c.426G>A|p.Ala142Ala |
S91 |
22 | BAA01g21990 | A01 | 10962970 | A | C | synonymous_variant | LOW | c.439A>C|p.Arg147Arg |
S91 |
23 | BAA01g21990 | A01 | 10962972 | G | T | missense_variant | MODERATE | c.441G>T|p.Arg147Ser |
S91 |
24 | BAA01g21990 | A01 | 10962984 | A | T | synonymous_variant | LOW | c.453A>T|p.Ser151Ser |
S91 |
25 | BAA01g21990 | A01 | 10962990 | G | C | synonymous_variant | LOW | c.459G>C|p.Ala153Ala |
S91 |