Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42040 | A09 | 48578792 | G | A | downstream_gene_variant | MODIFIER | c.*4566C>T| |
S280 |
2 | BAA09g42040 | A09 | 48579859 | G | A | downstream_gene_variant | MODIFIER | c.*3499C>T| |
S252 |
3 | BAA09g42040 | A09 | 48580618 | C | T | downstream_gene_variant | MODIFIER | c.*2740G>A| |
S5 |
4 | BAA09g42040 | A09 | 48581741 | C | T | downstream_gene_variant | MODIFIER | c.*1617G>A| |
S135 |
5 | BAA09g42040 | A09 | 48581839 | G | A | downstream_gene_variant | MODIFIER | c.*1519C>T| |
S88 |
6 | BAA09g42040 | A09 | 48582376 | G | A | downstream_gene_variant | MODIFIER | c.*982C>T| |
S76 |
7 | BAA09g42040 | A09 | 48583270 | C | T | downstream_gene_variant | MODIFIER | c.*88G>A| |
S36 |
8 | BAA09g42040 | A09 | 48583526 | G | A | synonymous_variant | LOW | c.1389C>T|p.Thr463Thr |
S217 |
9 | BAA09g42040 | A09 | 48584273 | C | T | missense_variant | MODERATE | c.1000G>A|p.Asp334Asn |
S77 S82 |
10 | BAA09g42040 | A09 | 48584492 | G | A | missense_variant | MODERATE | c.781C>T|p.Arg261Cys |
S189 |
11 | BAA09g42040 | A09 | 48587228 | C | T | upstream_gene_variant | MODIFIER | c.-1366G>A| |
S282 |
12 | BAA09g42040 | A09 | 48587589 | C | T | upstream_gene_variant | MODIFIER | c.-1727G>A| |
S125 |
13 | BAA09g42040 | A09 | 48587887 | G | A | upstream_gene_variant | MODIFIER | c.-2025C>T| |
S177 |
14 | BAA09g42040 | A09 | 48588408 | C | T | upstream_gene_variant | MODIFIER | c.-2546G>A| |
S261 |
15 | BAA09g42040 | A09 | 48588680 | G | A | upstream_gene_variant | MODIFIER | c.-2818C>T| |
S270 |
16 | BAA09g42040 | A09 | 48590260 | C | T | upstream_gene_variant | MODIFIER | c.-4398G>A| |
S6 |
17 | BAA09g42040 | A09 | 48590483 | C | T | upstream_gene_variant | MODIFIER | c.-4621G>A| |
S18 |