Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g00490 | A03 | 167108 | C | T | upstream_gene_variant | MODIFIER | c.-3252C>T| |
S143 S63 |
2 | BAA03g00490 | A03 | 167124 | C | T | upstream_gene_variant | MODIFIER | c.-3236C>T| |
S81 S85 |
3 | BAA03g00490 | A03 | 170463 | C | T | missense_variant | MODERATE | c.104C>T|p.Ser35Phe |
S245 |
4 | BAA03g00490 | A03 | 170586 | G | A | missense_variant | MODERATE | c.227G>A|p.Gly76Glu |
S155 S211 |
5 | BAA03g00490 | A03 | 170681 | C | T | missense_variant | MODERATE | c.322C>T|p.Leu108Phe |
S177 |
6 | BAA03g00490 | A03 | 171345 | C | T | splice_region_variant&intron_variant | LOW | c.528-6C>T| |
S132 S215 |
7 | BAA03g00490 | A03 | 173047 | G | A | synonymous_variant | LOW | c.1422G>A|p.Thr474Thr |
S213 |