Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g20440 | A03 | 9150837 | A | C | synonymous_variant | LOW | c.195A>C|p.Gly65Gly |
S23 |
2 | BAA03g20440 | A03 | 9150838 | A | C | missense_variant | MODERATE | c.196A>C|p.Asn66His |
S23 |
3 | BAA03g20440 | A03 | 9151741 | C | T | synonymous_variant | LOW | c.813C>T|p.Tyr271Tyr |
S234 |
4 | BAA03g20440 | A03 | 9151768 | C | T | synonymous_variant | LOW | c.840C>T|p.His280His |
S216 |
5 | BAA03g20440 | A03 | 9151904 | G | A | missense_variant | MODERATE | c.976G>A|p.Glu326Lys |
S142 |
6 | BAA03g20440 | A03 | 9152532 | C | T | missense_variant | MODERATE | c.1604C>T|p.Thr535Ile |
S106 |
7 | BAA03g20440 | A03 | 9152806 | G | A | synonymous_variant | LOW | c.1878G>A|p.Glu626Glu |
S33 |
8 | BAA03g20440 | A03 | 9152881 | C | T | synonymous_variant | LOW | c.1953C>T|p.Gly651Gly |
S82 S92 |