Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02990 | A08 | 2098628 | G | A | upstream_gene_variant | MODIFIER | c.-4953G>A| |
S97 |
2 | BAA08g02990 | A08 | 2098829 | C | T | upstream_gene_variant | MODIFIER | c.-4752C>T| |
S105 S106 |
3 | BAA08g02990 | A08 | 2098913 | G | A | upstream_gene_variant | MODIFIER | c.-4668G>A| |
S39 |
4 | BAA08g02990 | A08 | 2099458 | C | T | upstream_gene_variant | MODIFIER | c.-4123C>T| |
S278 |
5 | BAA08g02990 | A08 | 2099766 | C | T | upstream_gene_variant | MODIFIER | c.-3815C>T| |
S142 |
6 | BAA08g02990 | A08 | 2101560 | G | A | upstream_gene_variant | MODIFIER | c.-2021G>A| |
S200 S264 |
7 | BAA08g02990 | A08 | 2101833 | C | T | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S173 |
8 | BAA08g02990 | A08 | 2102389 | C | T | upstream_gene_variant | MODIFIER | c.-1192C>T| |
S113 |
9 | BAA08g02990 | A08 | 2102553 | C | T | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S302 |
10 | BAA08g02990 | A08 | 2103186 | G | A | upstream_gene_variant | MODIFIER | c.-395G>A| |
S37 |
11 | BAA08g02990 | A08 | 2103201 | A | C | upstream_gene_variant | MODIFIER | c.-380A>C| |
S162 S268 S34 S37 S99 |
12 | BAA08g02990 | A08 | 2103225 | C | T | upstream_gene_variant | MODIFIER | c.-356C>T| |
S206 S26 |
13 | BAA08g02990 | A08 | 2103611 | G | A | missense_variant | MODERATE | c.31G>A|p.Gly11Arg |
S95 |
14 | BAA08g02990 | A08 | 2104105 | G | A | stop_gained | HIGH | c.354G>A|p.Trp118* |
S115 |
15 | BAA08g02990 | A08 | 2105369 | C | T | downstream_gene_variant | MODIFIER | c.*1123C>T| |
S134 |
16 | BAA08g02990 | A08 | 2106675 | C | T | downstream_gene_variant | MODIFIER | c.*2429C>T| |
S80 |
17 | BAA08g02990 | A08 | 2107247 | C | T | downstream_gene_variant | MODIFIER | c.*3001C>T| |
S308 |