Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44000 | A01 | 29114527 | G | A | missense_variant | MODERATE | c.10G>A|p.Asp4Asn |
S117 |
2 | BAA01g44000 | A01 | 29114891 | C | T | missense_variant | MODERATE | c.374C>T|p.Ser125Phe |
S4 |
3 | BAA01g44000 | A01 | 29114965 | C | T | missense_variant | MODERATE | c.448C>T|p.Pro150Ser |
S153 S213 |
4 | BAA01g44000 | A01 | 29115406 | G | A | missense_variant&splice_region_variant | MODERATE | c.889G>A|p.Gly297Arg |
S143 |
5 | BAA01g44000 | A01 | 29116200 | G | A | missense_variant | MODERATE | c.1078G>A|p.Asp360Asn |
S98 |
6 | BAA01g44000 | A01 | 29117477 | G | A | synonymous_variant | LOW | c.1839G>A|p.Lys613Lys |
S1 S90 |
7 | BAA01g44000 | A01 | 29117702 | C | T | missense_variant | MODERATE | c.1979C>T|p.Pro660Leu |
S206 S26 |
8 | BAA01g44000 | A01 | 29120846 | C | T | downstream_gene_variant | MODIFIER | c.*1811C>T| |
S203 |
9 | BAA01g44000 | A01 | 29122080 | G | A | downstream_gene_variant | MODIFIER | c.*3045G>A| |
S122 |
10 | BAA01g44000 | A01 | 29122113 | C | T | downstream_gene_variant | MODIFIER | c.*3078C>T| |
S247 |
11 | BAA01g44000 | A01 | 29122159 | G | A | downstream_gene_variant | MODIFIER | c.*3124G>A| |
S123 |