Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g10190 | A06 | 5140017 | G | A | missense_variant | MODERATE | c.154G>A|p.Glu52Lys |
S71 |
2 | BAA06g10190 | A06 | 5140021 | C | T | missense_variant | MODERATE | c.158C>T|p.Ser53Phe |
S67 |
3 | BAA06g10190 | A06 | 5140045 | G | A | stop_gained | HIGH | c.182G>A|p.Trp61* |
S273 |
4 | BAA06g10190 | A06 | 5140075 | G | A | missense_variant | MODERATE | c.212G>A|p.Arg71Lys |
S125 |
5 | BAA06g10190 | A06 | 5141093 | G | A | missense_variant | MODERATE | c.847G>A|p.Asp283Asn |
S85 |
6 | BAA06g10190 | A06 | 5141177 | G | A | missense_variant | MODERATE | c.931G>A|p.Glu311Lys |
S165 |
7 | BAA06g10190 | A06 | 5141190 | G | A | missense_variant | MODERATE | c.944G>A|p.Arg315Lys |
S190 |
8 | BAA06g10190 | A06 | 5141458 | G | A | synonymous_variant | LOW | c.1212G>A|p.Ser404Ser |
S224 |
9 | BAA06g10190 | A06 | 5141735 | G | A | missense_variant | MODERATE | c.1489G>A|p.Glu497Lys |
S85 |
10 | BAA06g10190 | A06 | 5141805 | C | T | missense_variant | MODERATE | c.1559C>T|p.Ser520Phe |
S228 |