Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14980 | A10 | 15545970 | G | A | upstream_gene_variant | MODIFIER | c.-4291G>A| |
S155 S211 |
2 | BAA10g14980 | A10 | 15550755 | G | A | synonymous_variant | LOW | c.390G>A|p.Gln130Gln |
S234 |
3 | BAA10g14980 | A10 | 15550891 | G | A | missense_variant | MODERATE | c.526G>A|p.Val176Ile |
S64 |
4 | BAA10g14980 | A10 | 15553601 | G | A | missense_variant | MODERATE | c.2239G>A|p.Asp747Asn |
S9 |
5 | BAA10g14980 | A10 | 15553967 | C | T | missense_variant | MODERATE | c.2605C>T|p.Arg869Trp |
S45 |
6 | BAA10g14980 | A10 | 15554036 | G | A | missense_variant | MODERATE | c.2674G>A|p.Val892Ile |
S94 |
7 | BAA10g14980 | A10 | 15554222 | G | A | missense_variant | MODERATE | c.2860G>A|p.Val954Met |
S303 |
8 | BAA10g14980 | A10 | 15554237 | G | A | missense_variant | MODERATE | c.2875G>A|p.Val959Ile |
S289 |