Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17830 | A05 | 10111628 | C | T | downstream_gene_variant | MODIFIER | c.*4570G>A| |
S111 |
2 | BAA05g17830 | A05 | 10112165 | G | A | downstream_gene_variant | MODIFIER | c.*4033C>T| |
S247 |
3 | BAA05g17830 | A05 | 10112193 | C | T | downstream_gene_variant | MODIFIER | c.*4005G>A| |
S306 S308 |
4 | BAA05g17830 | A05 | 10112240 | C | T | downstream_gene_variant | MODIFIER | c.*3958G>A| |
S88 |
5 | BAA05g17830 | A05 | 10113072 | G | A | downstream_gene_variant | MODIFIER | c.*3126C>T| |
S75 S81 |
6 | BAA05g17830 | A05 | 10113755 | C | T | downstream_gene_variant | MODIFIER | c.*2443G>A| |
S5 |
7 | BAA05g17830 | A05 | 10114234 | G | A | downstream_gene_variant | MODIFIER | c.*1964C>T| |
S206 S26 |
8 | BAA05g17830 | A05 | 10114438 | C | T | downstream_gene_variant | MODIFIER | c.*1760G>A| |
S135 |
9 | BAA05g17830 | A05 | 10114794 | C | T | downstream_gene_variant | MODIFIER | c.*1404G>A| |
S130 |
10 | BAA05g17830 | A05 | 10115500 | C | T | downstream_gene_variant | MODIFIER | c.*698G>A| |
S137 S215 |
11 | BAA05g17830 | A05 | 10116780 | C | T | intron_variant | MODIFIER | c.693-11G>A| |
S177 |
12 | BAA05g17830 | A05 | 10118224 | G | A | missense_variant | MODERATE | c.139C>T|p.Leu47Phe |
S156 |
13 | BAA05g17830 | A05 | 10118676 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S15 |
14 | BAA05g17830 | A05 | 10119815 | C | T | upstream_gene_variant | MODIFIER | c.-1453G>A| |
S100 |
15 | BAA05g17830 | A05 | 10119977 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S239 |
16 | BAA05g17830 | A05 | 10120872 | G | A | upstream_gene_variant | MODIFIER | c.-2510C>T| |
S187 |
17 | BAA05g17830 | A05 | 10121187 | G | A | upstream_gene_variant | MODIFIER | c.-2825C>T| |
S241 |
18 | BAA05g17830 | A05 | 10121286 | G | A | upstream_gene_variant | MODIFIER | c.-2924C>T| |
S257 |