Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g14000 | A06 | 6915569 | G | A | missense_variant | MODERATE | c.1325C>T|p.Ser442Phe |
S166 |
2 | BAA06g14000 | A06 | 6916198 | G | A | missense_variant | MODERATE | c.1207C>T|p.Arg403Trp |
S308 |
3 | BAA06g14000 | A06 | 6916596 | C | T | synonymous_variant | LOW | c.1044G>A|p.Lys348Lys |
S272 |
4 | BAA06g14000 | A06 | 6917697 | C | T | missense_variant | MODERATE | c.823G>A|p.Gly275Ser |
S34 |
5 | BAA06g14000 | A06 | 6918466 | C | T | missense_variant | MODERATE | c.284G>A|p.Arg95Lys |
S230 |
6 | BAA06g14000 | A06 | 6919614 | G | A | upstream_gene_variant | MODIFIER | c.-609C>T| |
S262 |
7 | BAA06g14000 | A06 | 6919715 | G | A | upstream_gene_variant | MODIFIER | c.-710C>T| |
|
8 | BAA06g14000 | A06 | 6920277 | G | C | upstream_gene_variant | MODIFIER | c.-1272C>G| |
S100 |
9 | BAA06g14000 | A06 | 6920662 | C | T | upstream_gene_variant | MODIFIER | c.-1657G>A| |
S42 |
10 | BAA06g14000 | A06 | 6921160 | C | T | upstream_gene_variant | MODIFIER | c.-2155G>A| |
S99 |
11 | BAA06g14000 | A06 | 6921427 | G | A | upstream_gene_variant | MODIFIER | c.-2422C>T| |
S190 |
12 | BAA06g14000 | A06 | 6922363 | G | A | upstream_gene_variant | MODIFIER | c.-3358C>T| |
S179 |
13 | BAA06g14000 | A06 | 6923459 | C | T | upstream_gene_variant | MODIFIER | c.-4454G>A| |
S79 S84 |