Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26190 | A09 | 16963870 | C | T | downstream_gene_variant | MODIFIER | c.*3209G>A| |
S54 |
2 | BAA09g26190 | A09 | 16964483 | T | C | downstream_gene_variant | MODIFIER | c.*2596A>G| |
S136 S186 S275 S301 |
3 | BAA09g26190 | A09 | 16967035 | G | A | downstream_gene_variant | MODIFIER | c.*44C>T| |
S164 |
4 | BAA09g26190 | A09 | 16967729 | G | A | missense_variant | MODERATE | c.1372C>T|p.His458Tyr |
S224 |
5 | BAA09g26190 | A09 | 16967965 | G | A | missense_variant | MODERATE | c.1136C>T|p.Ala379Val |
S240 |
6 | BAA09g26190 | A09 | 16968496 | G | A | missense_variant | MODERATE | c.605C>T|p.Thr202Ile |
S146 |
7 | BAA09g26190 | A09 | 16968911 | G | A | stop_gained | HIGH | c.190C>T|p.Gln64* |
S224 |
8 | BAA09g26190 | A09 | 16968927 | G | A | synonymous_variant | LOW | c.174C>T|p.Thr58Thr |
S125 |
9 | BAA09g26190 | A09 | 16968957 | G | A | synonymous_variant | LOW | c.144C>T|p.Ile48Ile |
S265 |
10 | BAA09g26190 | A09 | 16969074 | G | A | synonymous_variant | LOW | c.27C>T|p.Leu9Leu |
S262 |
11 | BAA09g26190 | A09 | 16970308 | C | T | upstream_gene_variant | MODIFIER | c.-1208G>A| |
S5 S99 |
12 | BAA09g26190 | A09 | 16972383 | G | A | upstream_gene_variant | MODIFIER | c.-3283C>T| |
S262 |
13 | BAA09g26190 | A09 | 16972872 | G | A | upstream_gene_variant | MODIFIER | c.-3772C>T| |
S202 |
14 | BAA09g26190 | A09 | 16972971 | G | A | upstream_gene_variant | MODIFIER | c.-3871C>T| |
S40 S49 |
15 | BAA09g26190 | A09 | 16973283 | C | T | upstream_gene_variant | MODIFIER | c.-4183G>A| |
S234 |
16 | BAA09g26190 | A09 | 16973392 | G | A | upstream_gene_variant | MODIFIER | c.-4292C>T| |
S73 S91 |