Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00240 | A02 | 138977 | C | T | upstream_gene_variant | MODIFIER | c.-842C>T| |
S155 S211 |
2 | BAA02g00240 | A02 | 139916 | C | T | missense_variant | MODERATE | c.98C>T|p.Pro33Leu |
S221 |
3 | BAA02g00240 | A02 | 139967 | C | T | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S82 S92 |
4 | BAA02g00240 | A02 | 140744 | C | T | synonymous_variant | LOW | c.562C>T|p.Leu188Leu |
S177 |
5 | BAA02g00240 | A02 | 142267 | G | A | missense_variant | MODERATE | c.1214G>A|p.Ser405Asn |
S206 S26 |
6 | BAA02g00240 | A02 | 142401 | G | A | missense_variant | MODERATE | c.1348G>A|p.Gly450Arg |
S249 |
7 | BAA02g00240 | A02 | 142548 | G | A | missense_variant | MODERATE | c.1495G>A|p.Asp499Asn |
S153 S213 |
8 | BAA02g00240 | A02 | 143932 | G | A | intron_variant | MODIFIER | c.2245-131G>A| |
S165 |
9 | BAA02g00240 | A02 | 144189 | C | T | intron_variant | MODIFIER | c.2361+10C>T| |
S56 |
10 | BAA02g00240 | A02 | 145434 | C | T | missense_variant | MODERATE | c.2971C>T|p.Pro991Ser |
S82 S92 |
11 | BAA02g00240 | A02 | 145508 | G | A | synonymous_variant | LOW | c.3045G>A|p.Glu1015Glu |
S173 |
12 | BAA02g00240 | A02 | 146130 | G | A | missense_variant&splice_region_variant | MODERATE | c.3268G>A|p.Gly1090Arg |
S223 |
13 | BAA02g00240 | A02 | 146203 | G | A | missense_variant | MODERATE | c.3341G>A|p.Arg1114Lys |
S266 |
14 | BAA02g00240 | A02 | 147711 | G | A | missense_variant | MODERATE | c.4189G>A|p.Val1397Met |
S72 S78 |