Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42120 | A05 | 40018563 | C | T | missense_variant | MODERATE | c.2189G>A|p.Ser730Asn |
S256 |
2 | BAA05g42120 | A05 | 40021992 | C | T | missense_variant | MODERATE | c.1429G>A|p.Glu477Lys |
S62 |
3 | BAA05g42120 | A05 | 40022658 | G | A | missense_variant | MODERATE | c.1019C>T|p.Pro340Leu |
S19 |
4 | BAA05g42120 | A05 | 40022666 | C | T | synonymous_variant | LOW | c.1011G>A|p.Gly337Gly |
S170 |
5 | BAA05g42120 | A05 | 40024051 | C | T | missense_variant | MODERATE | c.313G>A|p.Glu105Lys |
S119 |
6 | BAA05g42120 | A05 | 40024054 | C | T | missense_variant | MODERATE | c.310G>A|p.Glu104Lys |
S165 |
7 | BAA05g42120 | A05 | 40024168 | C | T | missense_variant | MODERATE | c.196G>A|p.Glu66Lys |
S279 |
8 | BAA05g42120 | A05 | 40024291 | G | A | stop_gained | HIGH | c.73C>T|p.Gln25* |
S246 |
9 | BAA05g42120 | A05 | 40024318 | C | T | missense_variant | MODERATE | c.46G>A|p.Asp16Asn |
S128 |
10 | BAA05g42120 | A05 | 40024399 | G | A | upstream_gene_variant | MODIFIER | c.-36C>T| |
S211 S227 |
11 | BAA05g42120 | A05 | 40025796 | G | A | upstream_gene_variant | MODIFIER | c.-1433C>T| |
S250 |
12 | BAA05g42120 | A05 | 40025871 | G | A | upstream_gene_variant | MODIFIER | c.-1508C>T| |
S87 |
13 | BAA05g42120 | A05 | 40025917 | G | A | upstream_gene_variant | MODIFIER | c.-1554C>T| |
S296 |
14 | BAA05g42120 | A05 | 40027661 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S81 S85 |
15 | BAA05g42120 | A05 | 40028406 | C | T | upstream_gene_variant | MODIFIER | c.-4043G>A| |
S201 |
16 | BAA05g42120 | A05 | 40028487 | C | T | upstream_gene_variant | MODIFIER | c.-4124G>A| |
S295 |