Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11880 | A01 | 5557508 | G | A | downstream_gene_variant | MODIFIER | c.*3835C>T| |
S132 S89 |
2 | BAA01g11880 | A01 | 5557923 | C | T | downstream_gene_variant | MODIFIER | c.*3420G>A| |
S139 |
3 | BAA01g11880 | A01 | 5561696 | C | T | missense_variant | MODERATE | c.3034G>A|p.Gly1012Arg |
S16 |
4 | BAA01g11880 | A01 | 5562205 | C | T | missense_variant | MODERATE | c.2623G>A|p.Glu875Lys |
S78 |
5 | BAA01g11880 | A01 | 5563167 | C | T | synonymous_variant | LOW | c.1746G>A|p.Gln582Gln |
S286 |
6 | BAA01g11880 | A01 | 5563333 | G | A | missense_variant | MODERATE | c.1580C>T|p.Ser527Phe |
S67 |
7 | BAA01g11880 | A01 | 5563920 | C | T | synonymous_variant | LOW | c.1167G>A|p.Leu389Leu |
S148 S210 S30 S31 |
8 | BAA01g11880 | A01 | 5564423 | G | A | missense_variant | MODERATE | c.664C>T|p.Pro222Ser |
S252 |
9 | BAA01g11880 | A01 | 5565215 | C | T | synonymous_variant | LOW | c.219G>A|p.Leu73Leu |
S41 |
10 | BAA01g11880 | A01 | 5566008 | C | T | upstream_gene_variant | MODIFIER | c.-499G>A| |
S167 |
11 | BAA01g11880 | A01 | 5566170 | G | A | upstream_gene_variant | MODIFIER | c.-661C>T| |
S188 |
12 | BAA01g11880 | A01 | 5566173 | C | T | upstream_gene_variant | MODIFIER | c.-664G>A| |
S148 S30 S31 |