Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11110 | A08 | 9954311 | C | T | upstream_gene_variant | MODIFIER | c.-2583C>T| |
S76 |
2 | BAA08g11110 | A08 | 9955081 | G | A | upstream_gene_variant | MODIFIER | c.-1813G>A| |
S181 |
3 | BAA08g11110 | A08 | 9955206 | G | A | upstream_gene_variant | MODIFIER | c.-1688G>A| |
S2 S34 S4 |
4 | BAA08g11110 | A08 | 9955387 | G | A | upstream_gene_variant | MODIFIER | c.-1507G>A| |
S170 |
5 | BAA08g11110 | A08 | 9956024 | C | T | upstream_gene_variant | MODIFIER | c.-870C>T| |
S252 |
6 | BAA08g11110 | A08 | 9956673 | G | A | upstream_gene_variant | MODIFIER | c.-221G>A| |
S107 |
7 | BAA08g11110 | A08 | 9956798 | G | A | upstream_gene_variant | MODIFIER | c.-96G>A| |
S221 |
8 | BAA08g11110 | A08 | 9957048 | C | T | missense_variant | MODERATE | c.155C>T|p.Ala52Val |
S156 S276 |
9 | BAA08g11110 | A08 | 9957258 | C | T | missense_variant | MODERATE | c.365C>T|p.Ser122Phe |
S56 |
10 | BAA08g11110 | A08 | 9957981 | G | A | missense_variant | MODERATE | c.917G>A|p.Arg306Gln |
S146 |
11 | BAA08g11110 | A08 | 9959670 | G | T | missense_variant | MODERATE | c.1602G>T|p.Trp534Cys |
S61 |
12 | BAA08g11110 | A08 | 9960040 | G | A | missense_variant | MODERATE | c.1972G>A|p.Val658Met |
S246 |
13 | BAA08g11110 | A08 | 9960267 | G | A | intron_variant | MODIFIER | c.2173+26G>A| |
S81 S85 |
14 | BAA08g11110 | A08 | 9960294 | G | A | intron_variant | MODIFIER | c.2173+53G>A| |
S10 |
15 | BAA08g11110 | A08 | 9960669 | G | A | intron_variant | MODIFIER | c.2174-423G>A| |
S229 |
16 | BAA08g11110 | A08 | 9960887 | G | A | intron_variant | MODIFIER | c.2174-205G>A| |
S67 |
17 | BAA08g11110 | A08 | 9961414 | G | A | downstream_gene_variant | MODIFIER | c.*282G>A| |
S79 S91 |