Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39040 | A09 | 46763867 | G | A | upstream_gene_variant | MODIFIER | c.-4969G>A| |
S207 |
2 | BAA09g39040 | A09 | 46764152 | G | A | upstream_gene_variant | MODIFIER | c.-4684G>A| |
S160 |
3 | BAA09g39040 | A09 | 46764241 | C | T | upstream_gene_variant | MODIFIER | c.-4595C>T| |
S206 S26 S57 |
4 | BAA09g39040 | A09 | 46764551 | G | A | upstream_gene_variant | MODIFIER | c.-4285G>A| |
S167 |
5 | BAA09g39040 | A09 | 46764628 | C | T | upstream_gene_variant | MODIFIER | c.-4208C>T| |
S174 S27 |
6 | BAA09g39040 | A09 | 46765152 | C | T | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S6 |
7 | BAA09g39040 | A09 | 46765254 | G | A | upstream_gene_variant | MODIFIER | c.-3582G>A| |
S164 |
8 | BAA09g39040 | A09 | 46765357 | C | T | upstream_gene_variant | MODIFIER | c.-3479C>T| |
S138 |
9 | BAA09g39040 | A09 | 46765708 | C | T | upstream_gene_variant | MODIFIER | c.-3128C>T| |
S159 S243 S299 |
10 | BAA09g39040 | A09 | 46766529 | C | T | upstream_gene_variant | MODIFIER | c.-2307C>T| |
S292 |
11 | BAA09g39040 | A09 | 46766598 | C | T | upstream_gene_variant | MODIFIER | c.-2238C>T| |
S236 |
12 | BAA09g39040 | A09 | 46766692 | G | A | upstream_gene_variant | MODIFIER | c.-2144G>A| |
S288 |
13 | BAA09g39040 | A09 | 46766850 | C | T | upstream_gene_variant | MODIFIER | c.-1986C>T| |
S183 |
14 | BAA09g39040 | A09 | 46767011 | C | T | upstream_gene_variant | MODIFIER | c.-1825C>T| |
S136 |
15 | BAA09g39040 | A09 | 46767164 | C | T | upstream_gene_variant | MODIFIER | c.-1672C>T| |
S174 |
16 | BAA09g39040 | A09 | 46767626 | G | A | upstream_gene_variant | MODIFIER | c.-1210G>A| |
S281 |
17 | BAA09g39040 | A09 | 46769047 | C | T | missense_variant | MODERATE | c.212C>T|p.Thr71Ile |
S132 S137 |
18 | BAA09g39040 | A09 | 46773785 | C | T | downstream_gene_variant | MODIFIER | c.*4506C>T| |
S161 S228 S244 S289 |