Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02440 | A09 | 1585038 | G | A | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S107 |
2 | BAA09g02440 | A09 | 1586381 | T | G | start_lost | HIGH | c.2T>G|p.Met1? |
S132 S193 S198 S279 S301 S65 S67 |
3 | BAA09g02440 | A09 | 1586467 | G | A | missense_variant | MODERATE | c.88G>A|p.Asp30Asn |
S174 S216 S27 S39 |
4 | BAA09g02440 | A09 | 1586607 | C | T | synonymous_variant | LOW | c.228C>T|p.Asn76Asn |
S212 |
5 | BAA09g02440 | A09 | 1587497 | C | T | missense_variant | MODERATE | c.1118C>T|p.Thr373Ile |
S63 |
6 | BAA09g02440 | A09 | 1591091 | G | A | downstream_gene_variant | MODIFIER | c.*3524G>A| |
S295 |
7 | BAA09g02440 | A09 | 1591294 | G | A | downstream_gene_variant | MODIFIER | c.*3727G>A| |
S1 S161 S90 |
8 | BAA09g02440 | A09 | 1591454 | G | A | downstream_gene_variant | MODIFIER | c.*3887G>A| |
S241 |
9 | BAA09g02440 | A09 | 1591457 | G | A | downstream_gene_variant | MODIFIER | c.*3890G>A| |
S306 S308 |
10 | BAA09g02440 | A09 | 1592055 | G | A | downstream_gene_variant | MODIFIER | c.*4488G>A| |
S283 |