Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03400 | A10 | 1641462 | G | A | upstream_gene_variant | MODIFIER | c.-4720G>A| |
S136 |
2 | BAA10g03400 | A10 | 1641904 | G | A | upstream_gene_variant | MODIFIER | c.-4278G>A| |
S302 |
3 | BAA10g03400 | A10 | 1644240 | G | A | upstream_gene_variant | MODIFIER | c.-1942G>A| |
S94 |
4 | BAA10g03400 | A10 | 1644466 | G | A | upstream_gene_variant | MODIFIER | c.-1716G>A| |
S283 |
5 | BAA10g03400 | A10 | 1645127 | G | A | upstream_gene_variant | MODIFIER | c.-1055G>A| |
S76 |
6 | BAA10g03400 | A10 | 1645129 | G | A | upstream_gene_variant | MODIFIER | c.-1053G>A| |
S164 |
7 | BAA10g03400 | A10 | 1645629 | C | T | upstream_gene_variant | MODIFIER | c.-553C>T| |
S159 S243 S299 |
8 | BAA10g03400 | A10 | 1645970 | G | A | upstream_gene_variant | MODIFIER | c.-212G>A| |
S5 |
9 | BAA10g03400 | A10 | 1646367 | C | T | synonymous_variant | LOW | c.186C>T|p.Ile62Ile |
S125 |
10 | BAA10g03400 | A10 | 1647028 | C | T | missense_variant | MODERATE | c.610C>T|p.Leu204Phe |
S188 |