Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g21400 | A06 | 11486384 | G | A | missense_variant | MODERATE | c.1573C>T|p.Pro525Ser |
S133 |
2 | BAA06g21400 | A06 | 11486401 | C | T | missense_variant | MODERATE | c.1556G>A|p.Gly519Glu |
S231 |
3 | BAA06g21400 | A06 | 11487757 | C | T | missense_variant | MODERATE | c.550G>A|p.Ala184Thr |
S303 |
4 | BAA06g21400 | A06 | 11487767 | C | T | synonymous_variant | LOW | c.540G>A|p.Lys180Lys |
S56 |
5 | BAA06g21400 | A06 | 11488686 | C | T | missense_variant | MODERATE | c.106G>A|p.Val36Ile |
S183 S198 |
6 | BAA06g21400 | A06 | 11489096 | G | A | upstream_gene_variant | MODIFIER | c.-238C>T| |
S58 |
7 | BAA06g21400 | A06 | 11490598 | C | T | upstream_gene_variant | MODIFIER | c.-1740G>A| |
S68 |
8 | BAA06g21400 | A06 | 11490982 | G | A | upstream_gene_variant | MODIFIER | c.-2124C>T| |
S117 |
9 | BAA06g21400 | A06 | 11491009 | C | T | upstream_gene_variant | MODIFIER | c.-2151G>A| |
S286 |
10 | BAA06g21400 | A06 | 11491423 | C | T | upstream_gene_variant | MODIFIER | c.-2565G>A| |
S67 |
11 | BAA06g21400 | A06 | 11491699 | C | T | upstream_gene_variant | MODIFIER | c.-2841G>A| |
S25 |
12 | BAA06g21400 | A06 | 11491802 | G | A | upstream_gene_variant | MODIFIER | c.-2944C>T| |
S161 |
13 | BAA06g21400 | A06 | 11491922 | G | A | upstream_gene_variant | MODIFIER | c.-3064C>T| |
S274 |
14 | BAA06g21400 | A06 | 11492024 | G | A | upstream_gene_variant | MODIFIER | c.-3166C>T| |
S197 |
15 | BAA06g21400 | A06 | 11492627 | C | T | upstream_gene_variant | MODIFIER | c.-3769G>A| |
S286 |
16 | BAA06g21400 | A06 | 11492696 | C | T | upstream_gene_variant | MODIFIER | c.-3838G>A| |
S62 |
17 | BAA06g21400 | A06 | 11492726 | C | T | upstream_gene_variant | MODIFIER | c.-3868G>A| |
S179 |
18 | BAA06g21400 | A06 | 11493853 | C | T | upstream_gene_variant | MODIFIER | c.-4995G>A| |
S42 |