Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44110 | A02 | 36404125 | C | T | missense_variant | MODERATE | c.769G>A|p.Asp257Asn |
S65 |
2 | BAA02g44110 | A02 | 36404230 | G | A | missense_variant | MODERATE | c.664C>T|p.Pro222Ser |
S67 |
3 | BAA02g44110 | A02 | 36404395 | G | A | missense_variant | MODERATE | c.499C>T|p.Pro167Ser |
S82 S92 |
4 | BAA02g44110 | A02 | 36404650 | G | A | synonymous_variant | LOW | c.333C>T|p.Cys111Cys |
S293 |
5 | BAA02g44110 | A02 | 36404879 | C | T | missense_variant | MODERATE | c.104G>A|p.Gly35Glu |
S99 |
6 | BAA02g44110 | A02 | 36404986 | G | A | upstream_gene_variant | MODIFIER | c.-4C>T| |
S19 |
7 | BAA02g44110 | A02 | 36405420 | C | T | upstream_gene_variant | MODIFIER | c.-438G>A| |
S242 |
8 | BAA02g44110 | A02 | 36405514 | G | A | upstream_gene_variant | MODIFIER | c.-532C>T| |
S144 |
9 | BAA02g44110 | A02 | 36405836 | C | T | upstream_gene_variant | MODIFIER | c.-854G>A| |
S233 |
10 | BAA02g44110 | A02 | 36406101 | G | A | upstream_gene_variant | MODIFIER | c.-1119C>T| |
S77 S82 |
11 | BAA02g44110 | A02 | 36406132 | C | T | upstream_gene_variant | MODIFIER | c.-1150G>A| |
S195 |
12 | BAA02g44110 | A02 | 36406473 | C | T | upstream_gene_variant | MODIFIER | c.-1491G>A| |
S65 |
13 | BAA02g44110 | A02 | 36406611 | C | T | upstream_gene_variant | MODIFIER | c.-1629G>A| |
S283 |
14 | BAA02g44110 | A02 | 36407093 | C | T | upstream_gene_variant | MODIFIER | c.-2111G>A| |
S100 |
15 | BAA02g44110 | A02 | 36407976 | C | T | upstream_gene_variant | MODIFIER | c.-2994G>A| |
S115 |
16 | BAA02g44110 | A02 | 36408248 | C | T | upstream_gene_variant | MODIFIER | c.-3266G>A| |
S48 |