Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g46130 | A06 | 29349912 | G | A | downstream_gene_variant | MODIFIER | c.*2924C>T| |
S67 |
2 | BAA06g46130 | A06 | 29350033 | G | A | downstream_gene_variant | MODIFIER | c.*2803C>T| |
S202 |
3 | BAA06g46130 | A06 | 29352904 | G | A | missense_variant | MODERATE | c.2671C>T|p.Pro891Ser |
S88 |
4 | BAA06g46130 | A06 | 29352961 | C | T | missense_variant | MODERATE | c.2614G>A|p.Val872Met |
S34 |
5 | BAA06g46130 | A06 | 29352990 | G | A | missense_variant | MODERATE | c.2585C>T|p.Ser862Phe |
S54 |
6 | BAA06g46130 | A06 | 29353247 | G | A | synonymous_variant | LOW | c.2328C>T|p.Asp776Asp |
S59 |
7 | BAA06g46130 | A06 | 29354709 | G | A | stop_gained | HIGH | c.1255C>T|p.Gln419* |
S233 |
8 | BAA06g46130 | A06 | 29354889 | C | T | missense_variant | MODERATE | c.1075G>A|p.Ala359Thr |
S95 |
9 | BAA06g46130 | A06 | 29354982 | C | T | missense_variant | MODERATE | c.982G>A|p.Gly328Arg |
S297 |
10 | BAA06g46130 | A06 | 29355709 | C | T | synonymous_variant | LOW | c.621G>A|p.Ala207Ala |
S288 |
11 | BAA06g46130 | A06 | 29355872 | G | A | missense_variant | MODERATE | c.535C>T|p.Pro179Ser |
S12 |
12 | BAA06g46130 | A06 | 29356148 | G | A | synonymous_variant | LOW | c.259C>T|p.Leu87Leu |
S59 |
13 | BAA06g46130 | A06 | 29356467 | C | T | upstream_gene_variant | MODIFIER | c.-61G>A| |
S203 |
14 | BAA06g46130 | A06 | 29357091 | G | A | upstream_gene_variant | MODIFIER | c.-685C>T| |
S122 |
15 | BAA06g46130 | A06 | 29358897 | C | T | upstream_gene_variant | MODIFIER | c.-2491G>A| |
S297 |
16 | BAA06g46130 | A06 | 29360145 | C | T | upstream_gene_variant | MODIFIER | c.-3739G>A| |
S124 |