Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45660 | A02 | 37319280 | G | A | missense_variant | MODERATE | c.2645C>T|p.Ala882Val |
S266 |
2 | BAA02g45660 | A02 | 37320514 | G | A | missense_variant | MODERATE | c.1889C>T|p.Thr630Ile |
S192 |
3 | BAA02g45660 | A02 | 37321451 | C | T | missense_variant | MODERATE | c.1048G>A|p.Glu350Lys |
S33 |
4 | BAA02g45660 | A02 | 37321729 | C | T | missense_variant | MODERATE | c.770G>A|p.Gly257Glu |
S157 |
5 | BAA02g45660 | A02 | 37323223 | C | T | intron_variant | MODIFIER | c.121+24G>A| |
S270 |
6 | BAA02g45660 | A02 | 37323346 | C | T | missense_variant | MODERATE | c.22G>A|p.Glu8Lys |
S119 |
7 | BAA02g45660 | A02 | 37323886 | G | A | upstream_gene_variant | MODIFIER | c.-519C>T| |
S174 S216 |
8 | BAA02g45660 | A02 | 37325865 | C | T | upstream_gene_variant | MODIFIER | c.-2498G>A| |
S295 |
9 | BAA02g45660 | A02 | 37327361 | G | A | upstream_gene_variant | MODIFIER | c.-3994C>T| |
S223 |
10 | BAA02g45660 | A02 | 37327657 | G | A | upstream_gene_variant | MODIFIER | c.-4290C>T| |
S232 |
11 | BAA02g45660 | A02 | 37327783 | C | T | upstream_gene_variant | MODIFIER | c.-4416G>A| |
S242 |
12 | BAA02g45660 | A02 | 37328180 | G | A | upstream_gene_variant | MODIFIER | c.-4813C>T| |
S25 |