Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04790 | A09 | 2783946 | C | T | downstream_gene_variant | MODIFIER | c.*1495G>A| |
S183 S198 |
2 | BAA09g04790 | A09 | 2785670 | G | A | missense_variant | MODERATE | c.2135C>T|p.Ala712Val |
S85 |
3 | BAA09g04790 | A09 | 2785709 | G | A | missense_variant | MODERATE | c.2096C>T|p.Thr699Ile |
S174 S216 S27 S39 |
4 | BAA09g04790 | A09 | 2786205 | G | A | missense_variant | MODERATE | c.1717C>T|p.Pro573Ser |
S11 |
5 | BAA09g04790 | A09 | 2786460 | C | T | missense_variant | MODERATE | c.1462G>A|p.Gly488Arg |
S48 |
6 | BAA09g04790 | A09 | 2786753 | G | A | synonymous_variant | LOW | c.1254C>T|p.Leu418Leu |
S168 |
7 | BAA09g04790 | A09 | 2786837 | G | A | synonymous_variant | LOW | c.1170C>T|p.Tyr390Tyr |
S207 |
8 | BAA09g04790 | A09 | 2787285 | A | T | synonymous_variant | LOW | c.951T>A|p.Val317Val |
S115 |
9 | BAA09g04790 | A09 | 2788597 | G | A | synonymous_variant | LOW | c.627C>T|p.Tyr209Tyr |
S301 S304 |
10 | BAA09g04790 | A09 | 2789888 | G | A | upstream_gene_variant | MODIFIER | c.-115C>T| |
S201 |
11 | BAA09g04790 | A09 | 2789966 | G | A | upstream_gene_variant | MODIFIER | c.-193C>T| |
S40 S49 |
12 | BAA09g04790 | A09 | 2790175 | C | T | upstream_gene_variant | MODIFIER | c.-402G>A| |
S269 |
13 | BAA09g04790 | A09 | 2790244 | G | A | upstream_gene_variant | MODIFIER | c.-471C>T| |
S79 S84 |
14 | BAA09g04790 | A09 | 2791820 | G | A | upstream_gene_variant | MODIFIER | c.-2047C>T| |
S28 |
15 | BAA09g04790 | A09 | 2792919 | G | A | upstream_gene_variant | MODIFIER | c.-3146C>T| |
S57 |
16 | BAA09g04790 | A09 | 2794298 | G | A | upstream_gene_variant | MODIFIER | c.-4525C>T| |
S306 S308 |