Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12140 | A10 | 13616499 | C | T | downstream_gene_variant | MODIFIER | c.*3779G>A| |
S259 S42 |
2 | BAA10g12140 | A10 | 13617281 | C | T | downstream_gene_variant | MODIFIER | c.*2997G>A| |
S242 |
3 | BAA10g12140 | A10 | 13617391 | C | T | downstream_gene_variant | MODIFIER | c.*2887G>A| |
S282 |
4 | BAA10g12140 | A10 | 13620535 | T | G | missense_variant | MODERATE | c.1093A>C|p.Ile365Leu |
S109 S111 S158 S17 S180 S23 S248 S25 S262 S28 S291 |
5 | BAA10g12140 | A10 | 13620667 | C | T | missense_variant | MODERATE | c.961G>A|p.Gly321Arg |
S70 |
6 | BAA10g12140 | A10 | 13620757 | C | T | missense_variant | MODERATE | c.871G>A|p.Asp291Asn |
S149 |
7 | BAA10g12140 | A10 | 13621910 | G | A | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S138 |
8 | BAA10g12140 | A10 | 13622520 | G | A | upstream_gene_variant | MODIFIER | c.-409C>T| |
S290 |
9 | BAA10g12140 | A10 | 13625818 | C | T | upstream_gene_variant | MODIFIER | c.-3707G>A| |
S270 |
10 | BAA10g12140 | A10 | 13625822 | C | T | upstream_gene_variant | MODIFIER | c.-3711G>A| |
S8 |
11 | BAA10g12140 | A10 | 13626017 | C | T | upstream_gene_variant | MODIFIER | c.-3906G>A| |
S140 |
12 | BAA10g12140 | A10 | 13626828 | G | A | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S32 |
13 | BAA10g12140 | A10 | 13627081 | C | T | upstream_gene_variant | MODIFIER | c.-4970G>A| |
S25 |