Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18970 | A05 | 11045150 | G | A | downstream_gene_variant | MODIFIER | c.*2255C>T| |
S194 |
2 | BAA05g18970 | A05 | 11045307 | C | T | downstream_gene_variant | MODIFIER | c.*2098G>A| |
S186 |
3 | BAA05g18970 | A05 | 11045699 | C | T | downstream_gene_variant | MODIFIER | c.*1706G>A| |
S74 |
4 | BAA05g18970 | A05 | 11046016 | C | T | downstream_gene_variant | MODIFIER | c.*1389G>A| |
S17 |
5 | BAA05g18970 | A05 | 11046224 | C | T | downstream_gene_variant | MODIFIER | c.*1181G>A| |
S105 S106 |
6 | BAA05g18970 | A05 | 11046976 | G | A | downstream_gene_variant | MODIFIER | c.*429C>T| |
S23 |
7 | BAA05g18970 | A05 | 11047043 | G | A | downstream_gene_variant | MODIFIER | c.*362C>T| |
S107 |
8 | BAA05g18970 | A05 | 11047063 | C | T | downstream_gene_variant | MODIFIER | c.*342G>A| |
S58 |
9 | BAA05g18970 | A05 | 11047733 | G | A | missense_variant | MODERATE | c.1291C>T|p.Pro431Ser |
S158 |
10 | BAA05g18970 | A05 | 11047891 | C | T | missense_variant | MODERATE | c.1226G>A|p.Gly409Glu |
S146 |
11 | BAA05g18970 | A05 | 11048818 | G | A | synonymous_variant | LOW | c.744C>T|p.Asn248Asn |
S144 |
12 | BAA05g18970 | A05 | 11051761 | C | T | upstream_gene_variant | MODIFIER | c.-1524G>A| |
S306 S308 |
13 | BAA05g18970 | A05 | 11051777 | G | A | upstream_gene_variant | MODIFIER | c.-1540C>T| |
S79 S91 |
14 | BAA05g18970 | A05 | 11052381 | G | A | upstream_gene_variant | MODIFIER | c.-2144C>T| |
S127 |
15 | BAA05g18970 | A05 | 11052661 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S165 |