Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26240 | A09 | 17013178 | C | T | downstream_gene_variant | MODIFIER | c.*3068G>A| |
S120 |
2 | BAA09g26240 | A09 | 17013238 | C | T | downstream_gene_variant | MODIFIER | c.*3008G>A| |
S64 |
3 | BAA09g26240 | A09 | 17014676 | G | A | downstream_gene_variant | MODIFIER | c.*1570C>T| |
S20 |
4 | BAA09g26240 | A09 | 17014772 | G | A | downstream_gene_variant | MODIFIER | c.*1474C>T| |
S70 S8 |
5 | BAA09g26240 | A09 | 17015041 | C | T | downstream_gene_variant | MODIFIER | c.*1205G>A| |
S96 |
6 | BAA09g26240 | A09 | 17015145 | G | A | downstream_gene_variant | MODIFIER | c.*1101C>T| |
S66 |
7 | BAA09g26240 | A09 | 17015929 | G | A | downstream_gene_variant | MODIFIER | c.*317C>T| |
S33 |
8 | BAA09g26240 | A09 | 17016860 | C | T | intron_variant | MODIFIER | c.1398-53G>A| |
S48 |
9 | BAA09g26240 | A09 | 17017439 | G | A | missense_variant | MODERATE | c.1058C>T|p.Ser353Phe |
S244 |
10 | BAA09g26240 | A09 | 17017943 | C | T | missense_variant | MODERATE | c.796G>A|p.Glu266Lys |
S47 |
11 | BAA09g26240 | A09 | 17020652 | C | A | stop_gained | HIGH | c.82G>T|p.Glu28* |
S73 S91 |
12 | BAA09g26240 | A09 | 17021651 | C | T | upstream_gene_variant | MODIFIER | c.-812G>A| |
S124 |
13 | BAA09g26240 | A09 | 17021946 | A | T | upstream_gene_variant | MODIFIER | c.-1107T>A| |
S38 |
14 | BAA09g26240 | A09 | 17025453 | C | T | upstream_gene_variant | MODIFIER | c.-4614G>A| |
S15 S3 |
15 | BAA09g26240 | A09 | 17025747 | C | T | upstream_gene_variant | MODIFIER | c.-4908G>A| |
S255 |