Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g35290 | A01 | 23624211 | C | T | missense_variant | MODERATE | c.68C>T|p.Ser23Phe |
S139 |
2 | BAA01g35290 | A01 | 23624400 | C | T | missense_variant | MODERATE | c.257C>T|p.Ser86Phe |
S234 |
3 | BAA01g35290 | A01 | 23625017 | G | A | missense_variant | MODERATE | c.706G>A|p.Gly236Ser |
S135 |
4 | BAA01g35290 | A01 | 23626392 | G | A | missense_variant | MODERATE | c.1337G>A|p.Arg446Lys |
S158 |
5 | BAA01g35290 | A01 | 23626745 | C | T | missense_variant | MODERATE | c.1468C>T|p.Pro490Ser |
S286 |
6 | BAA01g35290 | A01 | 23626906 | G | A | missense_variant | MODERATE | c.1550G>A|p.Gly517Glu |
S202 |
7 | BAA01g35290 | A01 | 23626971 | G | A | missense_variant | MODERATE | c.1615G>A|p.Gly539Ser |
S244 |
8 | BAA01g35290 | A01 | 23628880 | G | A | downstream_gene_variant | MODIFIER | c.*1871G>A| |
S99 |
9 | BAA01g35290 | A01 | 23628932 | C | T | downstream_gene_variant | MODIFIER | c.*1923C>T| |
S153 |
10 | BAA01g35290 | A01 | 23629225 | G | A | downstream_gene_variant | MODIFIER | c.*2216G>A| |
S299 |
11 | BAA01g35290 | A01 | 23629226 | G | A | downstream_gene_variant | MODIFIER | c.*2217G>A| |
S60 |
12 | BAA01g35290 | A01 | 23629233 | C | T | downstream_gene_variant | MODIFIER | c.*2224C>T| |
S204 |
13 | BAA01g35290 | A01 | 23631785 | C | T | downstream_gene_variant | MODIFIER | c.*4776C>T| |
S213 |