Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40740 | A05 | 39251466 | G | A | missense_variant | MODERATE | c.62G>A|p.Arg21Gln |
S174 |
2 | BAA05g40740 | A05 | 39251665 | C | T | synonymous_variant | LOW | c.261C>T|p.Asn87Asn |
S64 |
3 | BAA05g40740 | A05 | 39251720 | G | A | missense_variant | MODERATE | c.316G>A|p.Val106Ile |
S157 |
4 | BAA05g40740 | A05 | 39251722 | C | T | synonymous_variant | LOW | c.318C>T|p.Val106Val |
S58 |
5 | BAA05g40740 | A05 | 39251752 | C | T | synonymous_variant | LOW | c.348C>T|p.Thr116Thr |
S167 |
6 | BAA05g40740 | A05 | 39251792 | G | A | missense_variant | MODERATE | c.388G>A|p.Glu130Lys |
S193 |
7 | BAA05g40740 | A05 | 39251864 | G | A | missense_variant | MODERATE | c.460G>A|p.Val154Met |
S200 |
8 | BAA05g40740 | A05 | 39252068 | G | A | missense_variant&splice_region_variant | MODERATE | c.664G>A|p.Glu222Lys |
S284 S36 |
9 | BAA05g40740 | A05 | 39252820 | C | T | missense_variant | MODERATE | c.1073C>T|p.Thr358Ile |
S271 |