Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g38350 | A01 | 25575238 | G | A | upstream_gene_variant | MODIFIER | c.-2900G>A| |
S173 |
2 | BAA01g38350 | A01 | 25578144 | C | T | missense_variant | MODERATE | c.7C>T|p.Leu3Phe |
S186 |
3 | BAA01g38350 | A01 | 25578257 | C | T | synonymous_variant | LOW | c.120C>T|p.Asp40Asp |
S10 |
4 | BAA01g38350 | A01 | 25578363 | C | T | missense_variant | MODERATE | c.226C>T|p.Pro76Ser |
S239 |
5 | BAA01g38350 | A01 | 25579463 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.568-1G>A| |
S13 |
6 | BAA01g38350 | A01 | 25579815 | C | T | missense_variant | MODERATE | c.797C>T|p.Ser266Phe |
S50 |
7 | BAA01g38350 | A01 | 25579885 | G | A | synonymous_variant | LOW | c.867G>A|p.Arg289Arg |
S20 |
8 | BAA01g38350 | A01 | 25579971 | G | A | missense_variant | MODERATE | c.953G>A|p.Arg318Lys |
S153 S157 S236 S257 S262 S263 |
9 | BAA01g38350 | A01 | 25580106 | C | T | missense_variant | MODERATE | c.1088C>T|p.Ser363Phe |
S303 |
10 | BAA01g38350 | A01 | 25580697 | C | T | missense_variant | MODERATE | c.1531C>T|p.Leu511Phe |
S209 |