Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02280 | A10 | 1084709 | G | A | missense_variant | MODERATE | c.1580C>T|p.Thr527Ile |
S9 |
2 | BAA10g02280 | A10 | 1084934 | C | T | missense_variant | MODERATE | c.1355G>A|p.Gly452Glu |
S87 |
3 | BAA10g02280 | A10 | 1085193 | C | T | missense_variant | MODERATE | c.1096G>A|p.Val366Met |
S233 |
4 | BAA10g02280 | A10 | 1085407 | C | T | synonymous_variant | LOW | c.882G>A|p.Ala294Ala |
S125 |
5 | BAA10g02280 | A10 | 1085686 | C | T | stop_gained | HIGH | c.603G>A|p.Trp201* |
S273 |
6 | BAA10g02280 | A10 | 1085695 | C | T | synonymous_variant | LOW | c.594G>A|p.Glu198Glu |
S6 |
7 | BAA10g02280 | A10 | 1085971 | G | A | synonymous_variant | LOW | c.318C>T|p.Leu106Leu |
S150 |
8 | BAA10g02280 | A10 | 1089622 | G | A | upstream_gene_variant | MODIFIER | c.-3334C>T| |
S55 |
9 | BAA10g02280 | A10 | 1089950 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S25 |
10 | BAA10g02280 | A10 | 1090246 | G | A | upstream_gene_variant | MODIFIER | c.-3958C>T| |
S69 |