Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05560 | A07 | 5131009 | G | A | missense_variant | MODERATE | c.2426C>T|p.Pro809Leu |
S44 |
2 | BAA07g05560 | A07 | 5131532 | G | A | missense_variant | MODERATE | c.1903C>T|p.Pro635Ser |
S187 |
3 | BAA07g05560 | A07 | 5132179 | G | A | missense_variant | MODERATE | c.1256C>T|p.Thr419Ile |
S84 S93 |
4 | BAA07g05560 | A07 | 5132498 | G | A | missense_variant | MODERATE | c.937C>T|p.Leu313Phe |
S187 |
5 | BAA07g05560 | A07 | 5133987 | C | T | upstream_gene_variant | MODIFIER | c.-425G>A| |
S47 |
6 | BAA07g05560 | A07 | 5134576 | C | T | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S241 S255 |
7 | BAA07g05560 | A07 | 5134928 | G | A | upstream_gene_variant | MODIFIER | c.-1366C>T| |
S229 |
8 | BAA07g05560 | A07 | 5135828 | C | T | upstream_gene_variant | MODIFIER | c.-2266G>A| |
S162 |
9 | BAA07g05560 | A07 | 5137427 | G | A | upstream_gene_variant | MODIFIER | c.-3865C>T| |
S44 |