Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g36180 | A07 | 33928952 | C | T | upstream_gene_variant | MODIFIER | c.-2826C>T| |
S239 S33 |
2 | BAA07g36180 | A07 | 33932115 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.170-1G>A| |
S210 |
3 | BAA07g36180 | A07 | 33932646 | G | A | missense_variant | MODERATE | c.619G>A|p.Gly207Ser |
S16 |
4 | BAA07g36180 | A07 | 33932673 | G | A | missense_variant | MODERATE | c.646G>A|p.Asp216Asn |
S76 |
5 | BAA07g36180 | A07 | 33932769 | C | T | missense_variant | MODERATE | c.742C>T|p.Pro248Ser |
S260 |
6 | BAA07g36180 | A07 | 33932854 | G | A | missense_variant | MODERATE | c.827G>A|p.Gly276Glu |
S126 |
7 | BAA07g36180 | A07 | 33932906 | G | A | synonymous_variant | LOW | c.879G>A|p.Glu293Glu |
S263 |
8 | BAA07g36180 | A07 | 33932926 | G | A | missense_variant | MODERATE | c.899G>A|p.Gly300Asp |
S271 |
9 | BAA07g36180 | A07 | 33937682 | C | T | downstream_gene_variant | MODIFIER | c.*4593C>T| |
S282 |