Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34040 | A02 | 29174462 | C | T | downstream_gene_variant | MODIFIER | c.*2950G>A| |
S221 |
2 | BAA02g34040 | A02 | 29175219 | C | T | downstream_gene_variant | MODIFIER | c.*2193G>A| |
S130 |
3 | BAA02g34040 | A02 | 29175511 | G | A | downstream_gene_variant | MODIFIER | c.*1901C>T| |
S217 |
4 | BAA02g34040 | A02 | 29175692 | C | T | downstream_gene_variant | MODIFIER | c.*1720G>A| |
S179 |
5 | BAA02g34040 | A02 | 29176415 | C | T | downstream_gene_variant | MODIFIER | c.*997G>A| |
S203 |
6 | BAA02g34040 | A02 | 29176495 | G | A | downstream_gene_variant | MODIFIER | c.*917C>T| |
S34 |
7 | BAA02g34040 | A02 | 29177483 | C | T | missense_variant | MODERATE | c.1123G>A|p.Gly375Arg |
S234 |
8 | BAA02g34040 | A02 | 29177713 | C | T | missense_variant | MODERATE | c.893G>A|p.Gly298Asp |
S138 S143 |
9 | BAA02g34040 | A02 | 29178005 | C | T | missense_variant | MODERATE | c.601G>A|p.Gly201Ser |
S164 |
10 | BAA02g34040 | A02 | 29180285 | A | G | upstream_gene_variant | MODIFIER | c.-1252T>C| |
S111 |
11 | BAA02g34040 | A02 | 29181270 | C | T | upstream_gene_variant | MODIFIER | c.-2237G>A| |
S183 S198 |
12 | BAA02g34040 | A02 | 29181498 | C | T | upstream_gene_variant | MODIFIER | c.-2465G>A| |
S276 |
13 | BAA02g34040 | A02 | 29181586 | C | T | upstream_gene_variant | MODIFIER | c.-2553G>A| |
S216 |
14 | BAA02g34040 | A02 | 29182332 | G | A | upstream_gene_variant | MODIFIER | c.-3299C>T| |
S168 |
15 | BAA02g34040 | A02 | 29182601 | C | T | upstream_gene_variant | MODIFIER | c.-3568G>A| |
S15 S3 |
16 | BAA02g34040 | A02 | 29182634 | C | T | upstream_gene_variant | MODIFIER | c.-3601G>A| |
S257 |