Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g65190 | A03 | 39347244 | C | T | upstream_gene_variant | MODIFIER | c.-4641C>T| |
S80 |
2 | BAA03g65190 | A03 | 39347579 | C | T | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S193 |
3 | BAA03g65190 | A03 | 39348150 | G | A | upstream_gene_variant | MODIFIER | c.-3735G>A| |
S168 |
4 | BAA03g65190 | A03 | 39350408 | G | A | upstream_gene_variant | MODIFIER | c.-1477G>A| |
S148 |
5 | BAA03g65190 | A03 | 39350420 | G | A | upstream_gene_variant | MODIFIER | c.-1465G>A| |
S27 |
6 | BAA03g65190 | A03 | 39351946 | G | A | missense_variant | MODERATE | c.62G>A|p.Gly21Asp |
S54 |
7 | BAA03g65190 | A03 | 39352226 | G | A | intron_variant | MODIFIER | c.224-17G>A| |
S73 S91 |
8 | BAA03g65190 | A03 | 39352342 | C | T | missense_variant | MODERATE | c.323C>T|p.Ala108Val |
S9 |
9 | BAA03g65190 | A03 | 39352656 | C | T | missense_variant | MODERATE | c.563C>T|p.Pro188Leu |
S45 |
10 | BAA03g65190 | A03 | 39352713 | C | T | missense_variant | MODERATE | c.596C>T|p.Ala199Val |
S293 |
11 | BAA03g65190 | A03 | 39353391 | C | T | downstream_gene_variant | MODIFIER | c.*317C>T| |
S4 |
12 | BAA03g65190 | A03 | 39353532 | C | T | downstream_gene_variant | MODIFIER | c.*458C>T| |
S156 |
13 | BAA03g65190 | A03 | 39353860 | C | T | downstream_gene_variant | MODIFIER | c.*786C>T| |
S38 |
14 | BAA03g65190 | A03 | 39355554 | C | T | downstream_gene_variant | MODIFIER | c.*2480C>T| |
S173 |
15 | BAA03g65190 | A03 | 39355753 | G | A | downstream_gene_variant | MODIFIER | c.*2679G>A| |
S46 |
16 | BAA03g65190 | A03 | 39356372 | G | A | downstream_gene_variant | MODIFIER | c.*3298G>A| |
S296 |
17 | BAA03g65190 | A03 | 39356831 | G | A | downstream_gene_variant | MODIFIER | c.*3757G>A| |
S203 |
18 | BAA03g65190 | A03 | 39356931 | G | A | downstream_gene_variant | MODIFIER | c.*3857G>A| |
S48 |