Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24940 | A09 | 16006675 | G | A | missense_variant | MODERATE | c.1985C>T|p.Thr662Ile |
S301 |
2 | BAA09g24940 | A09 | 16006694 | G | A | missense_variant | MODERATE | c.1966C>T|p.Leu656Phe |
S274 |
3 | BAA09g24940 | A09 | 16007808 | C | T | synonymous_variant | LOW | c.1227G>A|p.Thr409Thr |
S108 |
4 | BAA09g24940 | A09 | 16010187 | G | A | splice_region_variant&intron_variant | LOW | c.681-6C>T| |
S246 |
5 | BAA09g24940 | A09 | 16010243 | G | A | intron_variant | MODIFIER | c.681-62C>T| |
S303 |
6 | BAA09g24940 | A09 | 16011235 | G | A | missense_variant | MODERATE | c.434C>T|p.Ala145Val |
S291 |
7 | BAA09g24940 | A09 | 16011431 | C | T | missense_variant | MODERATE | c.238G>A|p.Glu80Lys |
S242 |
8 | BAA09g24940 | A09 | 16011720 | G | A | upstream_gene_variant | MODIFIER | c.-52C>T| |
S45 |
9 | BAA09g24940 | A09 | 16012589 | C | T | upstream_gene_variant | MODIFIER | c.-921G>A| |
S11 |
10 | BAA09g24940 | A09 | 16012612 | C | T | upstream_gene_variant | MODIFIER | c.-944G>A| |
S10 |
11 | BAA09g24940 | A09 | 16012756 | C | T | upstream_gene_variant | MODIFIER | c.-1088G>A| |
S14 |
12 | BAA09g24940 | A09 | 16012901 | C | T | upstream_gene_variant | MODIFIER | c.-1233G>A| |
S272 |
13 | BAA09g24940 | A09 | 16014787 | G | A | upstream_gene_variant | MODIFIER | c.-3119C>T| |
S157 S163 |
14 | BAA09g24940 | A09 | 16015231 | C | T | upstream_gene_variant | MODIFIER | c.-3563G>A| |
S153 |
15 | BAA09g24940 | A09 | 16015979 | C | T | upstream_gene_variant | MODIFIER | c.-4311G>A| |
S11 |
16 | BAA09g24940 | A09 | 16016340 | G | A | upstream_gene_variant | MODIFIER | c.-4672C>T| |
S204 |