Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16210 | A05 | 8941715 | C | T | missense_variant | MODERATE | c.1489G>A|p.Ala497Thr |
S155 |
2 | BAA05g16210 | A05 | 8941973 | G | A | missense_variant | MODERATE | c.1231C>T|p.Leu411Phe |
S238 |
3 | BAA05g16210 | A05 | 8942155 | G | A | missense_variant | MODERATE | c.1049C>T|p.Ser350Phe |
S293 |
4 | BAA05g16210 | A05 | 8942360 | C | T | missense_variant | MODERATE | c.844G>A|p.Val282Ile |
S47 |
5 | BAA05g16210 | A05 | 8942383 | G | A | missense_variant | MODERATE | c.821C>T|p.Ser274Phe |
S76 |
6 | BAA05g16210 | A05 | 8942507 | C | T | missense_variant | MODERATE | c.697G>A|p.Glu233Lys |
S9 |
7 | BAA05g16210 | A05 | 8942735 | C | T | missense_variant | MODERATE | c.469G>A|p.Ala157Thr |
S139 |
8 | BAA05g16210 | A05 | 8942737 | G | A | missense_variant | MODERATE | c.467C>T|p.Ala156Val |
S297 |
9 | BAA05g16210 | A05 | 8943012 | C | T | missense_variant | MODERATE | c.271G>A|p.Gly91Arg |
S136 |
10 | BAA05g16210 | A05 | 8943056 | C | T | missense_variant | MODERATE | c.227G>A|p.Gly76Glu |
S18 |
11 | BAA05g16210 | A05 | 8943099 | C | T | missense_variant | MODERATE | c.184G>A|p.Gly62Ser |
S148 S31 |
12 | BAA05g16210 | A05 | 8943118 | C | T | synonymous_variant | LOW | c.165G>A|p.Ala55Ala |
S47 |
13 | BAA05g16210 | A05 | 8946260 | G | A | upstream_gene_variant | MODIFIER | c.-2833C>T| |
S206 S26 |
14 | BAA05g16210 | A05 | 8946412 | G | A | upstream_gene_variant | MODIFIER | c.-2985C>T| |
S138 |
15 | BAA05g16210 | A05 | 8946665 | G | A | upstream_gene_variant | MODIFIER | c.-3238C>T| |
S298 |
16 | BAA05g16210 | A05 | 8947458 | C | T | upstream_gene_variant | MODIFIER | c.-4031G>A| |
S25 |
17 | BAA05g16210 | A05 | 8947693 | C | T | upstream_gene_variant | MODIFIER | c.-4266G>A| |
S63 |
18 | BAA05g16210 | A05 | 8948237 | C | T | upstream_gene_variant | MODIFIER | c.-4810G>A| |
S35 |