Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11710 | A01 | 5435112 | C | T | upstream_gene_variant | MODIFIER | c.-2939C>T| |
S296 |
2 | BAA01g11710 | A01 | 5436712 | A | T | upstream_gene_variant | MODIFIER | c.-1339A>T| |
S187 |
3 | BAA01g11710 | A01 | 5436813 | C | T | upstream_gene_variant | MODIFIER | c.-1238C>T| |
S250 |
4 | BAA01g11710 | A01 | 5437023 | G | A | upstream_gene_variant | MODIFIER | c.-1028G>A| |
S238 |
5 | BAA01g11710 | A01 | 5437362 | C | T | upstream_gene_variant | MODIFIER | c.-689C>T| |
S40 S49 |
6 | BAA01g11710 | A01 | 5437886 | G | A | upstream_gene_variant | MODIFIER | c.-165G>A| |
S116 |
7 | BAA01g11710 | A01 | 5437973 | C | T | upstream_gene_variant | MODIFIER | c.-78C>T| |
S135 |
8 | BAA01g11710 | A01 | 5439074 | G | A | missense_variant | MODERATE | c.557G>A|p.Gly186Glu |
S294 |
9 | BAA01g11710 | A01 | 5439187 | G | A | missense_variant | MODERATE | c.670G>A|p.Asp224Asn |
S165 |
10 | BAA01g11710 | A01 | 5442094 | G | A | downstream_gene_variant | MODIFIER | c.*2890G>A| |
S247 |
11 | BAA01g11710 | A01 | 5442226 | C | T | downstream_gene_variant | MODIFIER | c.*3022C>T| |
S202 |
12 | BAA01g11710 | A01 | 5442464 | C | T | downstream_gene_variant | MODIFIER | c.*3260C>T| |
S158 |
13 | BAA01g11710 | A01 | 5442718 | C | T | downstream_gene_variant | MODIFIER | c.*3514C>T| |
S206 S26 |
14 | BAA01g11710 | A01 | 5442790 | G | A | downstream_gene_variant | MODIFIER | c.*3586G>A| |
S241 |
15 | BAA01g11710 | A01 | 5443059 | G | A | downstream_gene_variant | MODIFIER | c.*3855G>A| |
S204 |
16 | BAA01g11710 | A01 | 5443733 | G | A | downstream_gene_variant | MODIFIER | c.*4529G>A| |
S262 |
17 | BAA01g11710 | A01 | 5443980 | G | A | downstream_gene_variant | MODIFIER | c.*4776G>A| |
S153 |