Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26310 | A01 | 14633190 | G | A | upstream_gene_variant | MODIFIER | c.-4029G>A| |
S116 S148 S295 S296 S30 S31 S54 |
2 | BAA01g26310 | A01 | 14633613 | C | T | upstream_gene_variant | MODIFIER | c.-3606C>T| |
S18 |
3 | BAA01g26310 | A01 | 14634500 | G | A | upstream_gene_variant | MODIFIER | c.-2719G>A| |
S203 |
4 | BAA01g26310 | A01 | 14634597 | C | T | upstream_gene_variant | MODIFIER | c.-2622C>T| |
S87 |
5 | BAA01g26310 | A01 | 14634837 | C | T | upstream_gene_variant | MODIFIER | c.-2382C>T| |
S176 |
6 | BAA01g26310 | A01 | 14636890 | G | A | upstream_gene_variant | MODIFIER | c.-329G>A| |
S59 |
7 | BAA01g26310 | A01 | 14637889 | G | A | synonymous_variant | LOW | c.312G>A|p.Leu104Leu |
S174 S216 |
8 | BAA01g26310 | A01 | 14637975 | G | A | intron_variant | MODIFIER | c.372+26G>A| |
S62 |
9 | BAA01g26310 | A01 | 14638070 | C | T | missense_variant | MODERATE | c.415C>T|p.His139Tyr |
S182 |
10 | BAA01g26310 | A01 | 14638835 | C | T | missense_variant | MODERATE | c.1112C>T|p.Pro371Leu |
S115 |
11 | BAA01g26310 | A01 | 14638947 | C | T | synonymous_variant | LOW | c.1224C>T|p.Phe408Phe |
S255 |
12 | BAA01g26310 | A01 | 14639113 | C | T | missense_variant | MODERATE | c.1390C>T|p.Leu464Phe |
S69 |
13 | BAA01g26310 | A01 | 14639201 | C | T | missense_variant | MODERATE | c.1478C>T|p.Ala493Val |
S231 |
14 | BAA01g26310 | A01 | 14639713 | G | A | downstream_gene_variant | MODIFIER | c.*142G>A| |
S159 S243 S276 S298 S299 |
15 | BAA01g26310 | A01 | 14640095 | G | A | downstream_gene_variant | MODIFIER | c.*524G>A| |
S278 |