Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08960 | A10 | 11008627 | G | A | upstream_gene_variant | MODIFIER | c.-4867G>A| |
S303 |
2 | BAA10g08960 | A10 | 11009148 | C | A | upstream_gene_variant | MODIFIER | c.-4346C>A| |
S8 |
3 | BAA10g08960 | A10 | 11011820 | G | A | upstream_gene_variant | MODIFIER | c.-1674G>A| |
S70 |
4 | BAA10g08960 | A10 | 11012527 | C | T | upstream_gene_variant | MODIFIER | c.-967C>T| |
S47 |
5 | BAA10g08960 | A10 | 11013651 | C | T | missense_variant | MODERATE | c.158C>T|p.Ser53Leu |
S297 |
6 | BAA10g08960 | A10 | 11013764 | G | A | missense_variant | MODERATE | c.271G>A|p.Gly91Ser |
S57 |
7 | BAA10g08960 | A10 | 11014105 | C | T | synonymous_variant | LOW | c.612C>T|p.Asp204Asp |
S176 |
8 | BAA10g08960 | A10 | 11014446 | G | A | missense_variant | MODERATE | c.929G>A|p.Gly310Glu |
S192 |
9 | BAA10g08960 | A10 | 11014488 | G | A | missense_variant | MODERATE | c.971G>A|p.Arg324Lys |
S140 |
10 | BAA10g08960 | A10 | 11014672 | G | A | intron_variant | MODIFIER | c.1144+11G>A| |
S251 |
11 | BAA10g08960 | A10 | 11014689 | G | A | intron_variant | MODIFIER | c.1144+28G>A| |
S138 |
12 | BAA10g08960 | A10 | 11016380 | G | A | downstream_gene_variant | MODIFIER | c.*1583G>A| |
S107 |
13 | BAA10g08960 | A10 | 11019412 | C | T | downstream_gene_variant | MODIFIER | c.*4615C>T| |
S166 |