Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g48760 | A03 | 23408321 | C | T | missense_variant | MODERATE | c.139C>T|p.Pro47Ser |
S15 S3 |
2 | BAA03g48760 | A03 | 23408645 | C | T | missense_variant | MODERATE | c.463C>T|p.Pro155Ser |
S183 S198 S240 |
3 | BAA03g48760 | A03 | 23408702 | G | A | missense_variant | MODERATE | c.520G>A|p.Glu174Lys |
S125 |
4 | BAA03g48760 | A03 | 23408751 | G | A | missense_variant | MODERATE | c.569G>A|p.Arg190Gln |
S256 |
5 | BAA03g48760 | A03 | 23408807 | G | A | missense_variant | MODERATE | c.625G>A|p.Glu209Lys |
S125 |
6 | BAA03g48760 | A03 | 23409274 | G | A | synonymous_variant | LOW | c.1092G>A|p.Lys364Lys |
S280 |
7 | BAA03g48760 | A03 | 23409963 | G | A | missense_variant | MODERATE | c.1703G>A|p.Cys568Tyr |
S233 |
8 | BAA03g48760 | A03 | 23410101 | G | A | missense_variant | MODERATE | c.1841G>A|p.Gly614Asp |
S17 |
9 | BAA03g48760 | A03 | 23410259 | G | A | missense_variant | MODERATE | c.1999G>A|p.Glu667Lys |
S168 S170 |
10 | BAA03g48760 | A03 | 23410403 | G | A | missense_variant | MODERATE | c.2143G>A|p.Gly715Arg |
S271 |
11 | BAA03g48760 | A03 | 23410609 | C | T | synonymous_variant | LOW | c.2349C>T|p.Ile783Ile |
S266 |