Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06140 | A01 | 2752024 | C | T | missense_variant | MODERATE | c.2335G>A|p.Gly779Arg |
S242 |
2 | BAA01g06140 | A01 | 2752273 | C | T | missense_variant | MODERATE | c.2086G>A|p.Val696Met |
S176 |
3 | BAA01g06140 | A01 | 2752475 | G | A | synonymous_variant | LOW | c.1884C>T|p.Ile628Ile |
S83 S88 |
4 | BAA01g06140 | A01 | 2752516 | C | A | missense_variant | MODERATE | c.1843G>T|p.Gly615Cys |
S68 |
5 | BAA01g06140 | A01 | 2753035 | C | T | missense_variant | MODERATE | c.1324G>A|p.Val442Ile |
S155 S211 |
6 | BAA01g06140 | A01 | 2753645 | C | T | synonymous_variant | LOW | c.714G>A|p.Glu238Glu |
S171 |
7 | BAA01g06140 | A01 | 2754093 | C | T | missense_variant | MODERATE | c.266G>A|p.Arg89Lys |
S125 |
8 | BAA01g06140 | A01 | 2754131 | G | A | synonymous_variant | LOW | c.228C>T|p.Ile76Ile |
S17 |
9 | BAA01g06140 | A01 | 2754159 | G | A | missense_variant | MODERATE | c.200C>T|p.Ser67Phe |
S293 |
10 | BAA01g06140 | A01 | 2756696 | G | A | upstream_gene_variant | MODIFIER | c.-2338C>T| |
S204 |
11 | BAA01g06140 | A01 | 2757375 | G | A | upstream_gene_variant | MODIFIER | c.-3017C>T| |
S190 |
12 | BAA01g06140 | A01 | 2758596 | G | A | upstream_gene_variant | MODIFIER | c.-4238C>T| |
S177 |
13 | BAA01g06140 | A01 | 2759153 | C | T | upstream_gene_variant | MODIFIER | c.-4795G>A| |
S104 S52 |