Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18900 | A05 | 10990902 | C | T | upstream_gene_variant | MODIFIER | c.-4199C>T| |
S69 |
2 | BAA05g18900 | A05 | 10991212 | C | T | upstream_gene_variant | MODIFIER | c.-3889C>T| |
S229 |
3 | BAA05g18900 | A05 | 10991312 | C | T | upstream_gene_variant | MODIFIER | c.-3789C>T| |
S89 |
4 | BAA05g18900 | A05 | 10994212 | C | T | upstream_gene_variant | MODIFIER | c.-889C>T| |
S89 |
5 | BAA05g18900 | A05 | 10994686 | G | A | upstream_gene_variant | MODIFIER | c.-415G>A| |
S139 |
6 | BAA05g18900 | A05 | 10994838 | G | A | upstream_gene_variant | MODIFIER | c.-263G>A| |
S292 |
7 | BAA05g18900 | A05 | 10994936 | G | A | upstream_gene_variant | MODIFIER | c.-165G>A| |
S288 |
8 | BAA05g18900 | A05 | 10995016 | C | T | upstream_gene_variant | MODIFIER | c.-85C>T| |
S241 |
9 | BAA05g18900 | A05 | 10995984 | C | T | synonymous_variant | LOW | c.405C>T|p.Ile135Ile |
S153 S213 S58 |
10 | BAA05g18900 | A05 | 10996252 | G | A | missense_variant | MODERATE | c.673G>A|p.Glu225Lys |
S3 |
11 | BAA05g18900 | A05 | 10996455 | C | T | synonymous_variant | LOW | c.876C>T|p.Tyr292Tyr |
S47 |
12 | BAA05g18900 | A05 | 10996784 | G | A | missense_variant | MODERATE | c.1132G>A|p.Ala378Thr |
S284 |
13 | BAA05g18900 | A05 | 10998377 | C | T | downstream_gene_variant | MODIFIER | c.*1501C>T| |
S247 |