Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00010 | A02 | 7511 | C | T | upstream_gene_variant | MODIFIER | c.-429C>T| |
S6 |
2 | BAA02g00010 | A02 | 8006 | C | T | missense_variant | MODERATE | c.67C>T|p.Pro23Ser |
S201 |
3 | BAA02g00010 | A02 | 8706 | G | A | missense_variant | MODERATE | c.527G>A|p.Gly176Glu |
S118 |
4 | BAA02g00010 | A02 | 8708 | G | A | missense_variant | MODERATE | c.529G>A|p.Gly177Arg |
S7 |
5 | BAA02g00010 | A02 | 9120 | C | T | intron_variant | MODIFIER | c.699-14C>T| |
S138 |
6 | BAA02g00010 | A02 | 9662 | C | T | intron_variant | MODIFIER | c.896+169C>T| |
S124 |
7 | BAA02g00010 | A02 | 10951 | G | A | intron_variant | MODIFIER | c.1087-594G>A| |
S10 |
8 | BAA02g00010 | A02 | 11271 | C | T | intron_variant | MODIFIER | c.1087-274C>T| |
S111 |
9 | BAA02g00010 | A02 | 11916 | C | T | intron_variant | MODIFIER | c.1171-40C>T| |
S306 |
10 | BAA02g00010 | A02 | 12001 | G | A | missense_variant | MODERATE | c.1216G>A|p.Asp406Asn |
S215 |