Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11630 | A04 | 17558545 | C | T | downstream_gene_variant | MODIFIER | c.*4824G>A| |
S293 |
2 | BAA04g11630 | A04 | 17558557 | C | T | downstream_gene_variant | MODIFIER | c.*4812G>A| |
S117 |
3 | BAA04g11630 | A04 | 17559191 | C | T | downstream_gene_variant | MODIFIER | c.*4178G>A| |
S239 |
4 | BAA04g11630 | A04 | 17559396 | C | T | downstream_gene_variant | MODIFIER | c.*3973G>A| |
S178 |
5 | BAA04g11630 | A04 | 17559605 | G | A | downstream_gene_variant | MODIFIER | c.*3764C>T| |
S109 |
6 | BAA04g11630 | A04 | 17559819 | C | T | downstream_gene_variant | MODIFIER | c.*3550G>A| |
S132 S137 S215 S89 |
7 | BAA04g11630 | A04 | 17559998 | C | T | downstream_gene_variant | MODIFIER | c.*3371G>A| |
S143 |
8 | BAA04g11630 | A04 | 17561164 | G | A | downstream_gene_variant | MODIFIER | c.*2205C>T| |
S124 |
9 | BAA04g11630 | A04 | 17562887 | G | A | downstream_gene_variant | MODIFIER | c.*482C>T| |
S162 |
10 | BAA04g11630 | A04 | 17563619 | C | T | missense_variant | MODERATE | c.419G>A|p.Arg140His |
S19 S305 S35 S5 |
11 | BAA04g11630 | A04 | 17564712 | A | T | upstream_gene_variant | MODIFIER | c.-569T>A| |
S64 |
12 | BAA04g11630 | A04 | 17564904 | C | T | upstream_gene_variant | MODIFIER | c.-761G>A| |
S185 |
13 | BAA04g11630 | A04 | 17564954 | G | A | upstream_gene_variant | MODIFIER | c.-811C>T| |
S85 |
14 | BAA04g11630 | A04 | 17565354 | G | A | upstream_gene_variant | MODIFIER | c.-1211C>T| |
S34 |
15 | BAA04g11630 | A04 | 17565544 | C | T | upstream_gene_variant | MODIFIER | c.-1401G>A| |
S118 |
16 | BAA04g11630 | A04 | 17566914 | C | T | upstream_gene_variant | MODIFIER | c.-2771G>A| |
S23 |
17 | BAA04g11630 | A04 | 17567457 | G | A | upstream_gene_variant | MODIFIER | c.-3314C>T| |
S193 |