Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06630 | A10 | 3491668 | G | A | downstream_gene_variant | MODIFIER | c.*4874C>T| |
S192 |
2 | BAA10g06630 | A10 | 3494239 | G | A | downstream_gene_variant | MODIFIER | c.*2303C>T| |
S295 |
3 | BAA10g06630 | A10 | 3496858 | G | A | missense_variant | MODERATE | c.1303C>T|p.Leu435Phe |
S45 |
4 | BAA10g06630 | A10 | 3497505 | G | A | intron_variant | MODIFIER | c.899+23C>T| |
S279 |
5 | BAA10g06630 | A10 | 3498215 | G | A | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S172 S217 |
6 | BAA10g06630 | A10 | 3498942 | C | T | intron_variant | MODIFIER | c.271-604G>A| |
S155 S211 |
7 | BAA10g06630 | A10 | 3499691 | C | T | intron_variant | MODIFIER | c.270+734G>A| |
S276 |
8 | BAA10g06630 | A10 | 3499792 | G | A | intron_variant | MODIFIER | c.270+633C>T| |
S184 |
9 | BAA10g06630 | A10 | 3501376 | G | A | upstream_gene_variant | MODIFIER | c.-682C>T| |
S12 |
10 | BAA10g06630 | A10 | 3501794 | C | T | upstream_gene_variant | MODIFIER | c.-1100G>A| |
S35 |
11 | BAA10g06630 | A10 | 3501861 | G | A | upstream_gene_variant | MODIFIER | c.-1167C>T| |
S292 |
12 | BAA10g06630 | A10 | 3503311 | C | T | upstream_gene_variant | MODIFIER | c.-2617G>A| |
S287 |
13 | BAA10g06630 | A10 | 3503546 | G | A | upstream_gene_variant | MODIFIER | c.-2852C>T| |
S4 |
14 | BAA10g06630 | A10 | 3503695 | C | T | upstream_gene_variant | MODIFIER | c.-3001G>A| |
S244 |