Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14260 | A02 | 6669951 | G | A | missense_variant | MODERATE | c.2054C>T|p.Pro685Leu |
S43 |
2 | BAA02g14260 | A02 | 6670061 | C | T | synonymous_variant | LOW | c.1944G>A|p.Lys648Lys |
S170 |
3 | BAA02g14260 | A02 | 6670164 | G | A | missense_variant | MODERATE | c.1841C>T|p.Ala614Val |
S23 |
4 | BAA02g14260 | A02 | 6670649 | G | A | missense_variant | MODERATE | c.1502C>T|p.Ala501Val |
S166 |
5 | BAA02g14260 | A02 | 6671328 | C | T | missense_variant | MODERATE | c.1183G>A|p.Gly395Ser |
S71 |
6 | BAA02g14260 | A02 | 6672124 | C | T | missense_variant | MODERATE | c.631G>A|p.Asp211Asn |
S272 |
7 | BAA02g14260 | A02 | 6672655 | C | T | missense_variant | MODERATE | c.100G>A|p.Ala34Thr |
S206 S26 |
8 | BAA02g14260 | A02 | 6673249 | G | A | upstream_gene_variant | MODIFIER | c.-495C>T| |
S190 |
9 | BAA02g14260 | A02 | 6673581 | G | A | upstream_gene_variant | MODIFIER | c.-827C>T| |
S192 |
10 | BAA02g14260 | A02 | 6673720 | C | T | upstream_gene_variant | MODIFIER | c.-966G>A| |
S182 |
11 | BAA02g14260 | A02 | 6674002 | G | A | upstream_gene_variant | MODIFIER | c.-1248C>T| |
S280 |
12 | BAA02g14260 | A02 | 6675022 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S202 |
13 | BAA02g14260 | A02 | 6677392 | G | A | upstream_gene_variant | MODIFIER | c.-4638C>T| |
S264 S293 |