Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26080 | A09 | 16879052 | G | A | missense_variant | MODERATE | c.50G>A|p.Gly17Glu |
S84 S93 |
2 | BAA09g26080 | A09 | 16879112 | G | A | splice_region_variant&intron_variant | LOW | c.106+4G>A| |
S287 |
3 | BAA09g26080 | A09 | 16879378 | C | T | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S148 S210 |
4 | BAA09g26080 | A09 | 16879928 | G | A | missense_variant | MODERATE | c.833G>A|p.Ser278Asn |
S25 |
5 | BAA09g26080 | A09 | 16880974 | G | A | synonymous_variant | LOW | c.1665G>A|p.Lys555Lys |
S289 |
6 | BAA09g26080 | A09 | 16881393 | C | T | missense_variant | MODERATE | c.2084C>T|p.Ser695Phe |
S156 |
7 | BAA09g26080 | A09 | 16881426 | G | A | missense_variant | MODERATE | c.2117G>A|p.Arg706Lys |
S238 |
8 | BAA09g26080 | A09 | 16881660 | C | T | missense_variant | MODERATE | c.2351C>T|p.Pro784Leu |
S282 |
9 | BAA09g26080 | A09 | 16881672 | G | A | missense_variant | MODERATE | c.2363G>A|p.Arg788Lys |
S116 S295 S30 S31 S54 |
10 | BAA09g26080 | A09 | 16881774 | C | T | missense_variant | MODERATE | c.2392C>T|p.His798Tyr |
S95 |
11 | BAA09g26080 | A09 | 16881947 | G | T | missense_variant | MODERATE | c.2565G>T|p.Lys855Asn |
S60 |