Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11880 | A06 | 6002518 | C | T | upstream_gene_variant | MODIFIER | c.-4489C>T| |
S116 |
2 | BAA06g11880 | A06 | 6003013 | C | T | upstream_gene_variant | MODIFIER | c.-3994C>T| |
S17 |
3 | BAA06g11880 | A06 | 6003379 | C | T | upstream_gene_variant | MODIFIER | c.-3628C>T| |
S205 |
4 | BAA06g11880 | A06 | 6003390 | G | A | upstream_gene_variant | MODIFIER | c.-3617G>A| |
S66 |
5 | BAA06g11880 | A06 | 6003462 | C | T | upstream_gene_variant | MODIFIER | c.-3545C>T| |
S281 |
6 | BAA06g11880 | A06 | 6003728 | G | A | upstream_gene_variant | MODIFIER | c.-3279G>A| |
S294 S75 S81 |
7 | BAA06g11880 | A06 | 6004255 | G | A | upstream_gene_variant | MODIFIER | c.-2752G>A| |
S68 |
8 | BAA06g11880 | A06 | 6004812 | C | T | upstream_gene_variant | MODIFIER | c.-2195C>T| |
S278 |
9 | BAA06g11880 | A06 | 6006741 | C | T | upstream_gene_variant | MODIFIER | c.-266C>T| |
S56 |
10 | BAA06g11880 | A06 | 6007293 | C | T | missense_variant | MODERATE | c.197C>T|p.Ser66Phe |
S148 S210 S31 |
11 | BAA06g11880 | A06 | 6007384 | C | T | intron_variant | MODIFIER | c.225-17C>T| |
S148 S210 S31 |
12 | BAA06g11880 | A06 | 6008715 | C | T | missense_variant | MODERATE | c.901C>T|p.Leu301Phe |
S231 |
13 | BAA06g11880 | A06 | 6008753 | C | T | synonymous_variant | LOW | c.939C>T|p.Phe313Phe |
S202 |
14 | BAA06g11880 | A06 | 6009285 | G | A | missense_variant | MODERATE | c.1202G>A|p.Gly401Glu |
S83 S88 |
15 | BAA06g11880 | A06 | 6010907 | C | T | downstream_gene_variant | MODIFIER | c.*1549C>T| |
S174 |