Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26570 | A01 | 14919490 | C | T | upstream_gene_variant | MODIFIER | c.-2778C>T| |
S273 |
2 | BAA01g26570 | A01 | 14920497 | C | T | upstream_gene_variant | MODIFIER | c.-1771C>T| |
S267 |
3 | BAA01g26570 | A01 | 14920554 | C | T | upstream_gene_variant | MODIFIER | c.-1714C>T| |
S277 |
4 | BAA01g26570 | A01 | 14921272 | C | T | upstream_gene_variant | MODIFIER | c.-996C>T| |
S200 |
5 | BAA01g26570 | A01 | 14921942 | G | A | upstream_gene_variant | MODIFIER | c.-326G>A| |
S32 |
6 | BAA01g26570 | A01 | 14922077 | C | T | upstream_gene_variant | MODIFIER | c.-191C>T| |
S117 |
7 | BAA01g26570 | A01 | 14922531 | G | A | synonymous_variant | LOW | c.264G>A|p.Ser88Ser |
S201 |
8 | BAA01g26570 | A01 | 14922620 | G | A | missense_variant | MODERATE | c.353G>A|p.Gly118Glu |
S187 |
9 | BAA01g26570 | A01 | 14922981 | G | A | synonymous_variant | LOW | c.714G>A|p.Ala238Ala |
S84 S93 |
10 | BAA01g26570 | A01 | 14923261 | G | A | missense_variant | MODERATE | c.994G>A|p.Asp332Asn |
S288 |
11 | BAA01g26570 | A01 | 14923424 | G | A | missense_variant | MODERATE | c.1157G>A|p.Arg386Lys |
S236 |
12 | BAA01g26570 | A01 | 14924210 | C | T | missense_variant | MODERATE | c.1649C>T|p.Pro550Leu |
S150 |
13 | BAA01g26570 | A01 | 14924849 | C | T | splice_region_variant&intron_variant | LOW | c.2199+7C>T| |
S117 |
14 | BAA01g26570 | A01 | 14930034 | C | T | downstream_gene_variant | MODIFIER | c.*4873C>T| |
S89 |