Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40340 | A01 | 26763432 | C | T | missense_variant | MODERATE | c.67C>T|p.Leu23Phe |
S157 |
2 | BAA01g40340 | A01 | 26764098 | C | T | synonymous_variant | LOW | c.733C>T|p.Leu245Leu |
S216 |
3 | BAA01g40340 | A01 | 26764758 | G | A | missense_variant | MODERATE | c.1393G>A|p.Glu465Lys |
S295 |
4 | BAA01g40340 | A01 | 26764958 | C | T | synonymous_variant | LOW | c.1593C>T|p.Val531Val |
S182 |
5 | BAA01g40340 | A01 | 26764992 | C | T | missense_variant | MODERATE | c.1627C>T|p.Pro543Ser |
S230 |
6 | BAA01g40340 | A01 | 26765239 | C | T | missense_variant | MODERATE | c.1874C>T|p.Pro625Leu |
S12 |
7 | BAA01g40340 | A01 | 26765417 | G | A | synonymous_variant | LOW | c.2052G>A|p.Gln684Gln |
S232 |
8 | BAA01g40340 | A01 | 26765754 | G | A | missense_variant&splice_region_variant | MODERATE | c.2323G>A|p.Glu775Lys |
S104 |
9 | BAA01g40340 | A01 | 26766375 | G | A | missense_variant | MODERATE | c.2866G>A|p.Val956Met |
S172 S217 |
10 | BAA01g40340 | A01 | 26766716 | G | A | synonymous_variant | LOW | c.3123G>A|p.Gly1041Gly |
S20 |
11 | BAA01g40340 | A01 | 26768135 | G | A | missense_variant | MODERATE | c.4294G>A|p.Asp1432Asn |
S179 |
12 | BAA01g40340 | A01 | 26768156 | C | T | missense_variant | MODERATE | c.4315C>T|p.Leu1439Phe |
S62 |
13 | BAA01g40340 | A01 | 26770509 | G | A | downstream_gene_variant | MODIFIER | c.*2142G>A| |
S234 |