Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15790 | A05 | 8535717 | C | T | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S266 |
2 | BAA05g15790 | A05 | 8536577 | G | A | missense_variant | MODERATE | c.682G>A|p.Gly228Ser |
S239 |
3 | BAA05g15790 | A05 | 8536751 | G | A | missense_variant | MODERATE | c.856G>A|p.Asp286Asn |
S37 |
4 | BAA05g15790 | A05 | 8537354 | T | A | missense_variant | MODERATE | c.1343T>A|p.Ile448Asn |
S128 |
5 | BAA05g15790 | A05 | 8538379 | C | T | downstream_gene_variant | MODIFIER | c.*862C>T| |
S237 |
6 | BAA05g15790 | A05 | 8538672 | C | T | downstream_gene_variant | MODIFIER | c.*1155C>T| |
S71 |
7 | BAA05g15790 | A05 | 8538746 | C | T | downstream_gene_variant | MODIFIER | c.*1229C>T| |
S114 |
8 | BAA05g15790 | A05 | 8538908 | G | A | downstream_gene_variant | MODIFIER | c.*1391G>A| |
S217 S248 |
9 | BAA05g15790 | A05 | 8538942 | G | A | downstream_gene_variant | MODIFIER | c.*1425G>A| |
S144 |
10 | BAA05g15790 | A05 | 8539013 | G | A | downstream_gene_variant | MODIFIER | c.*1496G>A| |
S293 |
11 | BAA05g15790 | A05 | 8539035 | C | T | downstream_gene_variant | MODIFIER | c.*1518C>T| |
S153 S213 |
12 | BAA05g15790 | A05 | 8539040 | G | A | downstream_gene_variant | MODIFIER | c.*1523G>A| |
S159 |
13 | BAA05g15790 | A05 | 8539746 | G | A | downstream_gene_variant | MODIFIER | c.*2229G>A| |
S197 |
14 | BAA05g15790 | A05 | 8540045 | C | T | downstream_gene_variant | MODIFIER | c.*2528C>T| |
S42 |
15 | BAA05g15790 | A05 | 8540662 | G | A | downstream_gene_variant | MODIFIER | c.*3145G>A| |
S54 |