Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38760 | A09 | 46497843 | C | T | downstream_gene_variant | MODIFIER | c.*3699G>A| |
S43 |
2 | BAA09g38760 | A09 | 46501509 | G | A | downstream_gene_variant | MODIFIER | c.*33C>T| |
S71 |
3 | BAA09g38760 | A09 | 46501960 | G | A | missense_variant | MODERATE | c.611C>T|p.Ser204Phe |
S156 |
4 | BAA09g38760 | A09 | 46502140 | C | T | missense_variant&splice_region_variant | MODERATE | c.512G>A|p.Gly171Glu |
S200 S303 |
5 | BAA09g38760 | A09 | 46502576 | C | T | intron_variant | MODIFIER | c.295-37G>A| |
S1 S90 |
6 | BAA09g38760 | A09 | 46503800 | C | T | upstream_gene_variant | MODIFIER | c.-508G>A| |
S86 |
7 | BAA09g38760 | A09 | 46503904 | C | T | upstream_gene_variant | MODIFIER | c.-612G>A| |
S192 |
8 | BAA09g38760 | A09 | 46504246 | C | T | upstream_gene_variant | MODIFIER | c.-954G>A| |
S193 |
9 | BAA09g38760 | A09 | 46504710 | C | T | upstream_gene_variant | MODIFIER | c.-1418G>A| |
S185 S273 |
10 | BAA09g38760 | A09 | 46504818 | G | A | upstream_gene_variant | MODIFIER | c.-1526C>T| |
S42 |
11 | BAA09g38760 | A09 | 46504878 | G | A | upstream_gene_variant | MODIFIER | c.-1586C>T| |
S149 |
12 | BAA09g38760 | A09 | 46505022 | C | T | upstream_gene_variant | MODIFIER | c.-1730G>A| |
S36 |
13 | BAA09g38760 | A09 | 46505026 | C | T | upstream_gene_variant | MODIFIER | c.-1734G>A| |
S202 |
14 | BAA09g38760 | A09 | 46505196 | C | T | upstream_gene_variant | MODIFIER | c.-1904G>A| |
S205 |
15 | BAA09g38760 | A09 | 46506128 | G | A | upstream_gene_variant | MODIFIER | c.-2836C>T| |
S244 |
16 | BAA09g38760 | A09 | 46508111 | C | T | upstream_gene_variant | MODIFIER | c.-4819G>A| |
S80 |