Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39030 | A01 | 25980024 | C | T | missense_variant | MODERATE | c.1129G>A|p.Glu377Lys |
S11 |
2 | BAA01g39030 | A01 | 25980099 | C | T | missense_variant | MODERATE | c.1054G>A|p.Asp352Asn |
S130 |
3 | BAA01g39030 | A01 | 25980270 | C | T | missense_variant | MODERATE | c.1003G>A|p.Glu335Lys |
S157 |
4 | BAA01g39030 | A01 | 25980388 | C | T | missense_variant | MODERATE | c.970G>A|p.Val324Ile |
S134 |
5 | BAA01g39030 | A01 | 25980412 | C | T | missense_variant | MODERATE | c.946G>A|p.Glu316Lys |
S153 |
6 | BAA01g39030 | A01 | 25980449 | C | T | stop_gained | HIGH | c.909G>A|p.Trp303* |
S240 |
7 | BAA01g39030 | A01 | 25980939 | C | T | missense_variant | MODERATE | c.599G>A|p.Arg200His |
S62 |
8 | BAA01g39030 | A01 | 25981025 | G | A | synonymous_variant | LOW | c.513C>T|p.Ser171Ser |
S157 S163 |
9 | BAA01g39030 | A01 | 25981616 | G | A | missense_variant | MODERATE | c.106C>T|p.Leu36Phe |
S223 |
10 | BAA01g39030 | A01 | 25981763 | G | A | upstream_gene_variant | MODIFIER | c.-42C>T| |
S209 |
11 | BAA01g39030 | A01 | 25981954 | G | T | upstream_gene_variant | MODIFIER | c.-233C>A| |
S212 S69 |
12 | BAA01g39030 | A01 | 25982494 | G | A | upstream_gene_variant | MODIFIER | c.-773C>T| |
S207 |
13 | BAA01g39030 | A01 | 25984321 | C | T | upstream_gene_variant | MODIFIER | c.-2600G>A| |
S270 |
14 | BAA01g39030 | A01 | 25984329 | C | T | upstream_gene_variant | MODIFIER | c.-2608G>A| |
S274 |
15 | BAA01g39030 | A01 | 25986373 | C | T | upstream_gene_variant | MODIFIER | c.-4652G>A| |
S56 |