Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26970 | A01 | 15244308 | C | T | missense_variant&splice_region_variant | MODERATE | c.3067G>A|p.Gly1023Arg |
S99 |
2 | BAA01g26970 | A01 | 15244362 | G | A | stop_gained | HIGH | c.3013C>T|p.Gln1005* |
S197 |
3 | BAA01g26970 | A01 | 15245180 | C | T | missense_variant | MODERATE | c.2492G>A|p.Arg831Lys |
S20 |
4 | BAA01g26970 | A01 | 15248452 | G | A | missense_variant | MODERATE | c.1423C>T|p.His475Tyr |
S23 |
5 | BAA01g26970 | A01 | 15249672 | C | T | synonymous_variant | LOW | c.369G>A|p.Glu123Glu |
S132 S137 S215 |
6 | BAA01g26970 | A01 | 15249870 | C | T | missense_variant | MODERATE | c.275G>A|p.Gly92Glu |
S120 |
7 | BAA01g26970 | A01 | 15250486 | C | T | upstream_gene_variant | MODIFIER | c.-239G>A| |
S89 |
8 | BAA01g26970 | A01 | 15252800 | G | A | upstream_gene_variant | MODIFIER | c.-2553C>T| |
S63 |
9 | BAA01g26970 | A01 | 15252816 | C | T | upstream_gene_variant | MODIFIER | c.-2569G>A| |
S42 |
10 | BAA01g26970 | A01 | 15252997 | C | T | upstream_gene_variant | MODIFIER | c.-2750G>A| |
S302 |
11 | BAA01g26970 | A01 | 15253481 | G | A | upstream_gene_variant | MODIFIER | c.-3234C>T| |
S294 |
12 | BAA01g26970 | A01 | 15254310 | C | A | upstream_gene_variant | MODIFIER | c.-4063G>T| |
S86 |
13 | BAA01g26970 | A01 | 15254640 | G | A | upstream_gene_variant | MODIFIER | c.-4393C>T| |
S172 |