Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10460 | A01 | 4791397 | C | T | synonymous_variant | LOW | c.759G>A|p.Glu253Glu |
S202 |
2 | BAA01g10460 | A01 | 4791399 | C | T | missense_variant | MODERATE | c.757G>A|p.Glu253Lys |
S183 |
3 | BAA01g10460 | A01 | 4791746 | G | A | missense_variant | MODERATE | c.410C>T|p.Ser137Phe |
S190 |
4 | BAA01g10460 | A01 | 4791816 | C | T | missense_variant | MODERATE | c.340G>A|p.Val114Ile |
S192 |
5 | BAA01g10460 | A01 | 4791827 | G | A | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S84 S93 |
6 | BAA01g10460 | A01 | 4792184 | C | T | synonymous_variant | LOW | c.153G>A|p.Pro51Pro |
S136 |
7 | BAA01g10460 | A01 | 4792194 | C | T | missense_variant | MODERATE | c.143G>A|p.Cys48Tyr |
S44 |
8 | BAA01g10460 | A01 | 4792212 | G | A | missense_variant | MODERATE | c.125C>T|p.Thr42Ile |
S1 S90 |
9 | BAA01g10460 | A01 | 4794060 | C | T | upstream_gene_variant | MODIFIER | c.-1724G>A| |
S198 |
10 | BAA01g10460 | A01 | 4794077 | G | A | upstream_gene_variant | MODIFIER | c.-1741C>T| |
S131 |
11 | BAA01g10460 | A01 | 4794280 | G | A | upstream_gene_variant | MODIFIER | c.-1944C>T| |
S69 |
12 | BAA01g10460 | A01 | 4794544 | G | A | upstream_gene_variant | MODIFIER | c.-2208C>T| |
S228 |
13 | BAA01g10460 | A01 | 4795295 | G | A | upstream_gene_variant | MODIFIER | c.-2959C>T| |
S80 |
14 | BAA01g10460 | A01 | 4795568 | C | T | upstream_gene_variant | MODIFIER | c.-3232G>A| |
S41 |
15 | BAA01g10460 | A01 | 4797037 | G | A | upstream_gene_variant | MODIFIER | c.-4701C>T| |
S172 S217 |