Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39180 | A09 | 46837312 | C | T | upstream_gene_variant | MODIFIER | c.-1238C>T| |
S143 |
2 | BAA09g39180 | A09 | 46838097 | C | T | upstream_gene_variant | MODIFIER | c.-453C>T| |
S104 S52 |
3 | BAA09g39180 | A09 | 46838671 | G | A | missense_variant | MODERATE | c.122G>A|p.Gly41Glu |
S280 |
4 | BAA09g39180 | A09 | 46838754 | G | A | missense_variant | MODERATE | c.205G>A|p.Glu69Lys |
S207 |
5 | BAA09g39180 | A09 | 46839275 | C | T | splice_region_variant&intron_variant | LOW | c.640+8C>T| |
S224 |
6 | BAA09g39180 | A09 | 46839627 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.754-1G>A| |
S134 |
7 | BAA09g39180 | A09 | 46840239 | C | T | missense_variant | MODERATE | c.1096C>T|p.Leu366Phe |
S28 |
8 | BAA09g39180 | A09 | 46840767 | G | A | missense_variant | MODERATE | c.1429G>A|p.Val477Ile |
S185 |
9 | BAA09g39180 | A09 | 46841251 | G | A | missense_variant | MODERATE | c.1651G>A|p.Glu551Lys |
S199 |
10 | BAA09g39180 | A09 | 46843026 | C | T | downstream_gene_variant | MODIFIER | c.*1659C>T| |
S139 |
11 | BAA09g39180 | A09 | 46844883 | G | A | downstream_gene_variant | MODIFIER | c.*3516G>A| |
S53 |