Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09050 | A05 | 4523470 | G | A | missense_variant | MODERATE | c.1411C>T|p.Arg471Cys |
S170 |
2 | BAA05g09050 | A05 | 4523682 | C | T | missense_variant | MODERATE | c.1199G>A|p.Gly400Glu |
S262 |
3 | BAA05g09050 | A05 | 4524385 | C | T | missense_variant | MODERATE | c.496G>A|p.Val166Met |
S201 |
4 | BAA05g09050 | A05 | 4524417 | C | T | missense_variant | MODERATE | c.464G>A|p.Gly155Asp |
S198 |
5 | BAA05g09050 | A05 | 4524701 | G | A | synonymous_variant | LOW | c.180C>T|p.Thr60Thr |
S40 S49 |
6 | BAA05g09050 | A05 | 4524714 | G | A | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S111 |
7 | BAA05g09050 | A05 | 4526457 | T | A | upstream_gene_variant | MODIFIER | c.-1577A>T| |
S177 |
8 | BAA05g09050 | A05 | 4526844 | G | A | upstream_gene_variant | MODIFIER | c.-1964C>T| |
S109 |
9 | BAA05g09050 | A05 | 4527220 | G | A | upstream_gene_variant | MODIFIER | c.-2340C>T| |
S298 |
10 | BAA05g09050 | A05 | 4528120 | C | T | upstream_gene_variant | MODIFIER | c.-3240G>A| |
S250 S291 |
11 | BAA05g09050 | A05 | 4528196 | C | T | upstream_gene_variant | MODIFIER | c.-3316G>A| |
S256 |
12 | BAA05g09050 | A05 | 4528601 | G | A | upstream_gene_variant | MODIFIER | c.-3721C>T| |
S107 |
13 | BAA05g09050 | A05 | 4528740 | G | T | upstream_gene_variant | MODIFIER | c.-3860C>A| |
S216 |