Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44060 | A01 | 29138787 | C | T | upstream_gene_variant | MODIFIER | c.-4140C>T| |
S23 |
2 | BAA01g44060 | A01 | 29139828 | G | A | upstream_gene_variant | MODIFIER | c.-3099G>A| |
S202 |
3 | BAA01g44060 | A01 | 29140008 | G | A | upstream_gene_variant | MODIFIER | c.-2919G>A| |
S33 |
4 | BAA01g44060 | A01 | 29142281 | C | T | upstream_gene_variant | MODIFIER | c.-646C>T| |
S58 |
5 | BAA01g44060 | A01 | 29142469 | C | T | upstream_gene_variant | MODIFIER | c.-458C>T| |
S19 |
6 | BAA01g44060 | A01 | 29142595 | C | T | upstream_gene_variant | MODIFIER | c.-332C>T| |
S19 |
7 | BAA01g44060 | A01 | 29142636 | C | T | upstream_gene_variant | MODIFIER | c.-291C>T| |
S233 |
8 | BAA01g44060 | A01 | 29143775 | C | T | intron_variant | MODIFIER | c.666+21C>T| |
S51 |
9 | BAA01g44060 | A01 | 29143890 | G | A | missense_variant | MODERATE | c.736G>A|p.Glu246Lys |
S272 |
10 | BAA01g44060 | A01 | 29144911 | G | A | missense_variant | MODERATE | c.1129G>A|p.Asp377Asn |
S53 |
11 | BAA01g44060 | A01 | 29145665 | C | T | missense_variant | MODERATE | c.1577C>T|p.Ala526Val |
S103 |
12 | BAA01g44060 | A01 | 29145895 | C | T | synonymous_variant | LOW | c.1710C>T|p.Phe570Phe |
S11 |
13 | BAA01g44060 | A01 | 29147763 | A | G | downstream_gene_variant | MODIFIER | c.*1555A>G| |
S59 |
14 | BAA01g44060 | A01 | 29149170 | C | T | downstream_gene_variant | MODIFIER | c.*2962C>T| |
S206 S26 |
15 | BAA01g44060 | A01 | 29149894 | C | T | downstream_gene_variant | MODIFIER | c.*3686C>T| |
S200 |
16 | BAA01g44060 | A01 | 29149952 | C | T | downstream_gene_variant | MODIFIER | c.*3744C>T| |
S8 |