Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11700 | A07 | 20354770 | G | A | downstream_gene_variant | MODIFIER | c.*4456C>T| |
S44 |
2 | BAA07g11700 | A07 | 20355097 | G | A | downstream_gene_variant | MODIFIER | c.*4129C>T| |
S122 |
3 | BAA07g11700 | A07 | 20355608 | G | A | downstream_gene_variant | MODIFIER | c.*3618C>T| |
S201 |
4 | BAA07g11700 | A07 | 20356149 | C | T | downstream_gene_variant | MODIFIER | c.*3077G>A| |
S169 |
5 | BAA07g11700 | A07 | 20356965 | G | A | downstream_gene_variant | MODIFIER | c.*2261C>T| |
S40 S49 |
6 | BAA07g11700 | A07 | 20357462 | C | T | downstream_gene_variant | MODIFIER | c.*1764G>A| |
S179 |
7 | BAA07g11700 | A07 | 20357604 | G | A | downstream_gene_variant | MODIFIER | c.*1622C>T| |
S157 S163 |
8 | BAA07g11700 | A07 | 20358686 | G | A | downstream_gene_variant | MODIFIER | c.*540C>T| |
S278 |
9 | BAA07g11700 | A07 | 20358875 | C | T | downstream_gene_variant | MODIFIER | c.*351G>A| |
S142 |
10 | BAA07g11700 | A07 | 20359261 | G | A | missense_variant | MODERATE | c.1015C>T|p.Pro339Ser |
S302 |
11 | BAA07g11700 | A07 | 20359802 | C | T | missense_variant | MODERATE | c.554G>A|p.Gly185Glu |
S11 |
12 | BAA07g11700 | A07 | 20360087 | C | T | missense_variant | MODERATE | c.269G>A|p.Arg90Gln |
S162 |
13 | BAA07g11700 | A07 | 20360151 | G | A | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S208 S219 |
14 | BAA07g11700 | A07 | 20360368 | C | T | upstream_gene_variant | MODIFIER | c.-13G>A| |
S232 |
15 | BAA07g11700 | A07 | 20360794 | C | T | upstream_gene_variant | MODIFIER | c.-439G>A| |
S167 |
16 | BAA07g11700 | A07 | 20362511 | C | T | upstream_gene_variant | MODIFIER | c.-2156G>A| |
S143 |
17 | BAA07g11700 | A07 | 20362942 | G | A | upstream_gene_variant | MODIFIER | c.-2587C>T| |
S124 |
18 | BAA07g11700 | A07 | 20365204 | G | A | upstream_gene_variant | MODIFIER | c.-4849C>T| |
S138 |
19 | BAA07g11700 | A07 | 20365224 | G | A | upstream_gene_variant | MODIFIER | c.-4869C>T| |
S159 |