Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20600 | A01 | 10169713 | T | G | downstream_gene_variant | MODIFIER | c.*3890A>C| |
S177 |
2 | BAA01g20600 | A01 | 10170470 | C | T | downstream_gene_variant | MODIFIER | c.*3133G>A| |
S257 |
3 | BAA01g20600 | A01 | 10170606 | C | T | downstream_gene_variant | MODIFIER | c.*2997G>A| |
S11 |
4 | BAA01g20600 | A01 | 10170696 | G | A | downstream_gene_variant | MODIFIER | c.*2907C>T| |
S6 |
5 | BAA01g20600 | A01 | 10170710 | C | T | downstream_gene_variant | MODIFIER | c.*2893G>A| |
S82 S92 |
6 | BAA01g20600 | A01 | 10171521 | C | T | downstream_gene_variant | MODIFIER | c.*2082G>A| |
S104 S52 |
7 | BAA01g20600 | A01 | 10171550 | G | A | downstream_gene_variant | MODIFIER | c.*2053C>T| |
S59 |
8 | BAA01g20600 | A01 | 10172624 | G | A | downstream_gene_variant | MODIFIER | c.*979C>T| |
S126 |
9 | BAA01g20600 | A01 | 10172758 | G | A | downstream_gene_variant | MODIFIER | c.*845C>T| |
S23 |
10 | BAA01g20600 | A01 | 10174690 | G | A | missense_variant | MODERATE | c.731C>T|p.Pro244Leu |
S209 |
11 | BAA01g20600 | A01 | 10175303 | G | A | missense_variant | MODERATE | c.118C>T|p.Pro40Ser |
S14 |
12 | BAA01g20600 | A01 | 10179915 | C | T | upstream_gene_variant | MODIFIER | c.-4495G>A| |
S63 |
13 | BAA01g20600 | A01 | 10180169 | G | A | upstream_gene_variant | MODIFIER | c.-4749C>T| |
S1 S90 |