Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09060 | A10 | 11119819 | C | T | downstream_gene_variant | MODIFIER | c.*3921G>A| |
S287 |
2 | BAA10g09060 | A10 | 11120186 | C | T | downstream_gene_variant | MODIFIER | c.*3554G>A| |
S270 |
3 | BAA10g09060 | A10 | 11120386 | C | T | downstream_gene_variant | MODIFIER | c.*3354G>A| |
S282 |
4 | BAA10g09060 | A10 | 11120465 | G | A | downstream_gene_variant | MODIFIER | c.*3275C>T| |
S161 |
5 | BAA10g09060 | A10 | 11120924 | G | A | downstream_gene_variant | MODIFIER | c.*2816C>T| |
S157 S163 |
6 | BAA10g09060 | A10 | 11121557 | C | T | downstream_gene_variant | MODIFIER | c.*2183G>A| |
S284 |
7 | BAA10g09060 | A10 | 11123457 | G | A | downstream_gene_variant | MODIFIER | c.*283C>T| |
S151 S263 |
8 | BAA10g09060 | A10 | 11124004 | C | T | synonymous_variant | LOW | c.1482G>A|p.Gln494Gln |
S17 |
9 | BAA10g09060 | A10 | 11124374 | G | A | intron_variant | MODIFIER | c.1289+39C>T| |
S125 |
10 | BAA10g09060 | A10 | 11125123 | C | T | missense_variant | MODERATE | c.878G>A|p.Gly293Glu |
S155 S211 |
11 | BAA10g09060 | A10 | 11125757 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.358-1G>A| |
S56 |
12 | BAA10g09060 | A10 | 11126194 | C | T | missense_variant | MODERATE | c.35G>A|p.Gly12Glu |
S10 |
13 | BAA10g09060 | A10 | 11128110 | G | A | upstream_gene_variant | MODIFIER | c.-1882C>T| |
S112 |
14 | BAA10g09060 | A10 | 11128399 | C | T | upstream_gene_variant | MODIFIER | c.-2171G>A| |
S133 |
15 | BAA10g09060 | A10 | 11128692 | C | T | upstream_gene_variant | MODIFIER | c.-2464G>A| |
S96 |
16 | BAA10g09060 | A10 | 11130395 | C | T | upstream_gene_variant | MODIFIER | c.-4167G>A| |
S201 |
17 | BAA10g09060 | A10 | 11130950 | C | T | upstream_gene_variant | MODIFIER | c.-4722G>A| |
S206 S26 |
18 | BAA10g09060 | A10 | 11130970 | A | C | upstream_gene_variant | MODIFIER | c.-4742T>G| |
S112 S286 S301 S5 |
19 | BAA10g09060 | A10 | 11130977 | G | A | upstream_gene_variant | MODIFIER | c.-4749C>T| |
S284 |