Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08770 | A02 | 3878262 | G | A | missense_variant | MODERATE | c.311G>A|p.Arg104Lys |
S79 S91 |
2 | BAA02g08770 | A02 | 3878706 | G | A | missense_variant | MODERATE | c.553G>A|p.Ala185Thr |
S97 |
3 | BAA02g08770 | A02 | 3878896 | G | A | missense_variant&splice_region_variant | MODERATE | c.655G>A|p.Gly219Arg |
S266 |
4 | BAA02g08770 | A02 | 3879229 | C | T | intron_variant | MODIFIER | c.781+17C>T| |
S195 |
5 | BAA02g08770 | A02 | 3879908 | C | T | missense_variant | MODERATE | c.1175C>T|p.Pro392Leu |
S104 |
6 | BAA02g08770 | A02 | 3880013 | G | A | missense_variant | MODERATE | c.1280G>A|p.Ser427Asn |
S84 S93 |
7 | BAA02g08770 | A02 | 3880016 | G | A | missense_variant | MODERATE | c.1283G>A|p.Gly428Glu |
S209 |
8 | BAA02g08770 | A02 | 3881010 | C | T | missense_variant | MODERATE | c.1700C>T|p.Ser567Phe |
S78 |
9 | BAA02g08770 | A02 | 3881573 | C | T | missense_variant | MODERATE | c.1942C>T|p.His648Tyr |
S167 |
10 | BAA02g08770 | A02 | 3881719 | G | A | missense_variant | MODERATE | c.2005G>A|p.Glu669Lys |
S204 |
11 | BAA02g08770 | A02 | 3881755 | G | A | missense_variant | MODERATE | c.2041G>A|p.Glu681Lys |
S37 |
12 | BAA02g08770 | A02 | 3882234 | C | T | synonymous_variant | LOW | c.2355C>T|p.Pro785Pro |
S263 |
13 | BAA02g08770 | A02 | 3882481 | G | A | missense_variant | MODERATE | c.2398G>A|p.Glu800Lys |
S139 |
14 | BAA02g08770 | A02 | 3885575 | C | T | downstream_gene_variant | MODIFIER | c.*2903C>T| |
S16 |