Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g40320 | A06 | 26226918 | G | A | downstream_gene_variant | MODIFIER | c.*4676C>T| |
S213 |
2 | BAA06g40320 | A06 | 26226940 | C | T | downstream_gene_variant | MODIFIER | c.*4654G>A| |
S174 S27 S74 |
3 | BAA06g40320 | A06 | 26227236 | C | T | downstream_gene_variant | MODIFIER | c.*4358G>A| |
S142 |
4 | BAA06g40320 | A06 | 26227415 | C | T | downstream_gene_variant | MODIFIER | c.*4179G>A| |
S81 S85 |
5 | BAA06g40320 | A06 | 26228122 | G | A | downstream_gene_variant | MODIFIER | c.*3472C>T| |
S263 |
6 | BAA06g40320 | A06 | 26228949 | G | A | downstream_gene_variant | MODIFIER | c.*2645C>T| |
S268 |
7 | BAA06g40320 | A06 | 26229771 | G | A | downstream_gene_variant | MODIFIER | c.*1823C>T| |
S271 |
8 | BAA06g40320 | A06 | 26230555 | C | T | downstream_gene_variant | MODIFIER | c.*1039G>A| |
S12 |
9 | BAA06g40320 | A06 | 26230756 | G | A | downstream_gene_variant | MODIFIER | c.*838C>T| |
S39 |
10 | BAA06g40320 | A06 | 26231430 | C | T | downstream_gene_variant | MODIFIER | c.*164G>A| |
S303 |
11 | BAA06g40320 | A06 | 26231626 | G | A | missense_variant | MODERATE | c.1132C>T|p.Pro378Ser |
S78 S83 |
12 | BAA06g40320 | A06 | 26231671 | G | A | missense_variant | MODERATE | c.1087C>T|p.Pro363Ser |
S233 |
13 | BAA06g40320 | A06 | 26231722 | G | A | missense_variant | MODERATE | c.1036C>T|p.Leu346Phe |
S32 |
14 | BAA06g40320 | A06 | 26231759 | C | T | synonymous_variant | LOW | c.999G>A|p.Gln333Gln |
S249 |
15 | BAA06g40320 | A06 | 26231983 | C | T | missense_variant | MODERATE | c.877G>A|p.Asp293Asn |
S115 |
16 | BAA06g40320 | A06 | 26234578 | G | A | stop_gained | HIGH | c.202C>T|p.Gln68* |
S219 S72 |
17 | BAA06g40320 | A06 | 26234591 | G | A | synonymous_variant | LOW | c.189C>T|p.Ser63Ser |
S203 |
18 | BAA06g40320 | A06 | 26234616 | G | A | missense_variant | MODERATE | c.164C>T|p.Ser55Phe |
S262 |
19 | BAA06g40320 | A06 | 26239477 | G | A | upstream_gene_variant | MODIFIER | c.-4698C>T| |
S87 |