Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26430 | A04 | 27006840 | G | A | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S186 |
2 | BAA04g26430 | A04 | 27008061 | C | T | upstream_gene_variant | MODIFIER | c.-396C>T| |
S243 S299 |
3 | BAA04g26430 | A04 | 27012575 | C | T | missense_variant | MODERATE | c.785C>T|p.Ser262Phe |
S112 |
4 | BAA04g26430 | A04 | 27012650 | C | T | missense_variant | MODERATE | c.860C>T|p.Ala287Val |
S151 S263 |
5 | BAA04g26430 | A04 | 27012848 | C | T | synonymous_variant | LOW | c.906C>T|p.Pro302Pro |
S246 |
6 | BAA04g26430 | A04 | 27013930 | G | A | missense_variant | MODERATE | c.1348G>A|p.Ala450Thr |
S263 |
7 | BAA04g26430 | A04 | 27014875 | G | A | missense_variant | MODERATE | c.1856G>A|p.Arg619His |
S297 |
8 | BAA04g26430 | A04 | 27014906 | G | A | missense_variant | MODERATE | c.1887G>A|p.Met629Ile |
S13 |
9 | BAA04g26430 | A04 | 27015116 | G | A | synonymous_variant | LOW | c.2097G>A|p.Gln699Gln |
S25 |
10 | BAA04g26430 | A04 | 27015134 | G | A | missense_variant | MODERATE | c.2115G>A|p.Met705Ile |
S18 |