Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20040 | A06 | 10490827 | C | T | missense_variant | MODERATE | c.1808G>A|p.Gly603Asp |
S150 |
2 | BAA06g20040 | A06 | 10490852 | A | C | missense_variant | MODERATE | c.1783T>G|p.Leu595Val |
S116 |
3 | BAA06g20040 | A06 | 10491456 | G | A | synonymous_variant | LOW | c.1560C>T|p.Arg520Arg |
S45 |
4 | BAA06g20040 | A06 | 10492148 | C | T | synonymous_variant | LOW | c.1221G>A|p.Leu407Leu |
S11 |
5 | BAA06g20040 | A06 | 10492156 | G | A | missense_variant | MODERATE | c.1213C>T|p.Pro405Ser |
S219 S72 |
6 | BAA06g20040 | A06 | 10492786 | C | T | synonymous_variant | LOW | c.900G>A|p.Thr300Thr |
S156 |
7 | BAA06g20040 | A06 | 10493181 | G | A | missense_variant | MODERATE | c.649C>T|p.Pro217Ser |
S224 |
8 | BAA06g20040 | A06 | 10495182 | C | T | upstream_gene_variant | MODIFIER | c.-1049G>A| |
S76 |
9 | BAA06g20040 | A06 | 10495234 | G | A | upstream_gene_variant | MODIFIER | c.-1101C>T| |
S69 |
10 | BAA06g20040 | A06 | 10495431 | C | T | upstream_gene_variant | MODIFIER | c.-1298G>A| |
S124 S146 |
11 | BAA06g20040 | A06 | 10496749 | C | T | upstream_gene_variant | MODIFIER | c.-2616G>A| |
S120 |
12 | BAA06g20040 | A06 | 10496856 | C | T | upstream_gene_variant | MODIFIER | c.-2723G>A| |
S67 |
13 | BAA06g20040 | A06 | 10497531 | C | T | upstream_gene_variant | MODIFIER | c.-3398G>A| |
S298 |
14 | BAA06g20040 | A06 | 10498194 | C | T | upstream_gene_variant | MODIFIER | c.-4061G>A| |
S46 |
15 | BAA06g20040 | A06 | 10498427 | G | A | upstream_gene_variant | MODIFIER | c.-4294C>T| |
S35 |
16 | BAA06g20040 | A06 | 10498494 | C | T | upstream_gene_variant | MODIFIER | c.-4361G>A| |
S247 |
17 | BAA06g20040 | A06 | 10498635 | C | T | upstream_gene_variant | MODIFIER | c.-4502G>A| |
S120 |
18 | BAA06g20040 | A06 | 10499095 | G | A | upstream_gene_variant | MODIFIER | c.-4962C>T| |
S72 S78 |