Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06060 | A07 | 15371414 | C | T | upstream_gene_variant | MODIFIER | c.-410C>T| |
S13 |
2 | BAA07g06060 | A07 | 15371447 | T | A | upstream_gene_variant | MODIFIER | c.-377T>A| |
S216 |
3 | BAA07g06060 | A07 | 15372084 | C | T | missense_variant | MODERATE | c.134C>T|p.Ser45Phe |
S174 |
4 | BAA07g06060 | A07 | 15372297 | C | T | missense_variant | MODERATE | c.347C>T|p.Ser116Phe |
S8 |
5 | BAA07g06060 | A07 | 15373081 | G | A | missense_variant | MODERATE | c.862G>A|p.Glu288Lys |
S255 |
6 | BAA07g06060 | A07 | 15373904 | G | A | intron_variant | MODIFIER | c.1194+400G>A| |
S43 |
7 | BAA07g06060 | A07 | 15374346 | G | A | intron_variant | MODIFIER | c.1195-491G>A| |
S158 |
8 | BAA07g06060 | A07 | 15374411 | G | A | intron_variant | MODIFIER | c.1195-426G>A| |
S10 |
9 | BAA07g06060 | A07 | 15374485 | G | A | intron_variant | MODIFIER | c.1195-352G>A| |
S193 |
10 | BAA07g06060 | A07 | 15374741 | G | A | intron_variant | MODIFIER | c.1195-96G>A| |
S281 |
11 | BAA07g06060 | A07 | 15374786 | G | A | intron_variant | MODIFIER | c.1195-51G>A| |
S237 |
12 | BAA07g06060 | A07 | 15374874 | G | A | missense_variant | MODERATE | c.1232G>A|p.Ser411Asn |
S272 |
13 | BAA07g06060 | A07 | 15374895 | C | T | missense_variant | MODERATE | c.1253C>T|p.Ser418Phe |
S195 |
14 | BAA07g06060 | A07 | 15375100 | C | T | downstream_gene_variant | MODIFIER | c.*141C>T| |
S96 |
15 | BAA07g06060 | A07 | 15375281 | C | T | downstream_gene_variant | MODIFIER | c.*322C>T| |
S249 |
16 | BAA07g06060 | A07 | 15375992 | C | T | downstream_gene_variant | MODIFIER | c.*1033C>T| |
S133 |