Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20500 | A09 | 12678048 | G | A | synonymous_variant | LOW | c.468G>A|p.Lys156Lys |
S301 S304 |
2 | BAA09g20500 | A09 | 12678526 | G | A | missense_variant | MODERATE | c.946G>A|p.Glu316Lys |
S211 |
3 | BAA09g20500 | A09 | 12679198 | G | A | missense_variant | MODERATE | c.1618G>A|p.Asp540Asn |
S157 S163 |
4 | BAA09g20500 | A09 | 12679252 | G | A | missense_variant | MODERATE | c.1672G>A|p.Asp558Asn |
S195 |
5 | BAA09g20500 | A09 | 12679865 | G | A | missense_variant | MODERATE | c.1915G>A|p.Glu639Lys |
S207 |
6 | BAA09g20500 | A09 | 12682057 | C | T | intron_variant | MODIFIER | c.2400+1707C>T| |
S39 |
7 | BAA09g20500 | A09 | 12682777 | C | T | intron_variant | MODIFIER | c.2401-1596C>T| |
S108 |
8 | BAA09g20500 | A09 | 12683296 | G | A | intron_variant | MODIFIER | c.2401-1077G>A| |
S38 |
9 | BAA09g20500 | A09 | 12686490 | G | A | missense_variant | MODERATE | c.3574G>A|p.Asp1192Asn |
S84 S93 |
10 | BAA09g20500 | A09 | 12687268 | G | A | downstream_gene_variant | MODIFIER | c.*189G>A| |
S205 |
11 | BAA09g20500 | A09 | 12688597 | G | A | downstream_gene_variant | MODIFIER | c.*1518G>A| |
S124 |
12 | BAA09g20500 | A09 | 12689267 | C | T | downstream_gene_variant | MODIFIER | c.*2188C>T| |
S256 S270 |
13 | BAA09g20500 | A09 | 12689410 | C | T | downstream_gene_variant | MODIFIER | c.*2331C>T| |
S293 |
14 | BAA09g20500 | A09 | 12690084 | G | A | downstream_gene_variant | MODIFIER | c.*3005G>A| |
S20 |
15 | BAA09g20500 | A09 | 12690323 | C | T | downstream_gene_variant | MODIFIER | c.*3244C>T| |
S160 |
16 | BAA09g20500 | A09 | 12690457 | C | T | downstream_gene_variant | MODIFIER | c.*3378C>T| |
S255 |