Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g26100 | A07 | 28505730 | C | T | downstream_gene_variant | MODIFIER | c.*3902G>A| |
S174 |
2 | BAA07g26100 | A07 | 28507560 | C | T | downstream_gene_variant | MODIFIER | c.*2072G>A| |
S190 |
3 | BAA07g26100 | A07 | 28509690 | G | A | missense_variant | MODERATE | c.1427C>T|p.Ser476Leu |
S187 |
4 | BAA07g26100 | A07 | 28509950 | C | T | missense_variant | MODERATE | c.1285G>A|p.Ala429Thr |
S77 S82 |
5 | BAA07g26100 | A07 | 28510213 | C | T | missense_variant | MODERATE | c.1093G>A|p.Glu365Lys |
S58 |
6 | BAA07g26100 | A07 | 28510775 | G | A | missense_variant | MODERATE | c.607C>T|p.His203Tyr |
S303 |
7 | BAA07g26100 | A07 | 28510945 | C | T | synonymous_variant | LOW | c.531G>A|p.Lys177Lys |
S8 |
8 | BAA07g26100 | A07 | 28512476 | G | A | upstream_gene_variant | MODIFIER | c.-795C>T| |
S188 |
9 | BAA07g26100 | A07 | 28513275 | C | T | upstream_gene_variant | MODIFIER | c.-1594G>A| |
S169 |
10 | BAA07g26100 | A07 | 28513289 | C | T | upstream_gene_variant | MODIFIER | c.-1608G>A| |
S206 |
11 | BAA07g26100 | A07 | 28514010 | G | A | upstream_gene_variant | MODIFIER | c.-2329C>T| |
S295 |
12 | BAA07g26100 | A07 | 28514856 | G | A | upstream_gene_variant | MODIFIER | c.-3175C>T| |
S262 |
13 | BAA07g26100 | A07 | 28515432 | C | T | upstream_gene_variant | MODIFIER | c.-3751G>A| |
S206 |
14 | BAA07g26100 | A07 | 28516183 | C | T | upstream_gene_variant | MODIFIER | c.-4502G>A| |
S293 |
15 | BAA07g26100 | A07 | 28516522 | G | A | upstream_gene_variant | MODIFIER | c.-4841C>T| |
S105 S106 |