Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g18400 | A06 | 9420430 | G | A | missense_variant | MODERATE | c.2885C>T|p.Thr962Ile |
S82 S92 |
2 | BAA06g18400 | A06 | 9420594 | G | A | synonymous_variant | LOW | c.2721C>T|p.Pro907Pro |
S139 |
3 | BAA06g18400 | A06 | 9421231 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2428-1G>A| |
S135 |
4 | BAA06g18400 | A06 | 9421576 | C | T | missense_variant | MODERATE | c.2158G>A|p.Val720Ile |
S239 |
5 | BAA06g18400 | A06 | 9422146 | C | T | missense_variant | MODERATE | c.1994G>A|p.Arg665His |
S159 S243 S299 |
6 | BAA06g18400 | A06 | 9423394 | G | A | missense_variant | MODERATE | c.1190C>T|p.Ala397Val |
S32 |
7 | BAA06g18400 | A06 | 9424046 | C | T | missense_variant | MODERATE | c.538G>A|p.Ala180Thr |
S167 |
8 | BAA06g18400 | A06 | 9425189 | C | T | upstream_gene_variant | MODIFIER | c.-190G>A| |
S157 |
9 | BAA06g18400 | A06 | 9425737 | G | A | upstream_gene_variant | MODIFIER | c.-738C>T| |
S237 |
10 | BAA06g18400 | A06 | 9426007 | G | A | upstream_gene_variant | MODIFIER | c.-1008C>T| |
S88 |
11 | BAA06g18400 | A06 | 9427824 | C | T | upstream_gene_variant | MODIFIER | c.-2825G>A| |
S178 |
12 | BAA06g18400 | A06 | 9429598 | G | A | upstream_gene_variant | MODIFIER | c.-4599C>T| |
S23 |