Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05150 | A07 | 4438148 | G | A | upstream_gene_variant | MODIFIER | c.-4696G>A| |
S132 S137 S215 |
2 | BAA07g05150 | A07 | 4439509 | G | A | upstream_gene_variant | MODIFIER | c.-3335G>A| |
S111 |
3 | BAA07g05150 | A07 | 4439555 | G | A | upstream_gene_variant | MODIFIER | c.-3289G>A| |
S87 |
4 | BAA07g05150 | A07 | 4440258 | G | A | upstream_gene_variant | MODIFIER | c.-2586G>A| |
S65 |
5 | BAA07g05150 | A07 | 4440642 | C | T | upstream_gene_variant | MODIFIER | c.-2202C>T| |
S162 |
6 | BAA07g05150 | A07 | 4440840 | T | C | upstream_gene_variant | MODIFIER | c.-2004T>C| |
S28 |
7 | BAA07g05150 | A07 | 4440930 | C | T | upstream_gene_variant | MODIFIER | c.-1914C>T| |
S197 |
8 | BAA07g05150 | A07 | 4441345 | G | A | upstream_gene_variant | MODIFIER | c.-1499G>A| |
S45 |
9 | BAA07g05150 | A07 | 4442900 | C | T | synonymous_variant | LOW | c.57C>T|p.Pro19Pro |
S86 |
10 | BAA07g05150 | A07 | 4443016 | C | T | missense_variant | MODERATE | c.173C>T|p.Ser58Leu |
S167 S205 |
11 | BAA07g05150 | A07 | 4443519 | G | A | missense_variant | MODERATE | c.676G>A|p.Gly226Ser |
S25 |
12 | BAA07g05150 | A07 | 4444384 | C | T | missense_variant | MODERATE | c.1541C>T|p.Thr514Ile |
S128 |
13 | BAA07g05150 | A07 | 4444419 | G | A | missense_variant | MODERATE | c.1576G>A|p.Gly526Arg |
S229 |
14 | BAA07g05150 | A07 | 4449919 | G | A | downstream_gene_variant | MODIFIER | c.*4646G>A| |
S180 |