Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g42790 | A03 | 20246952 | G | A | synonymous_variant | LOW | c.3195C>T|p.Leu1065Leu |
S68 |
2 | BAA03g42790 | A03 | 20247234 | G | A | synonymous_variant | LOW | c.2913C>T|p.Ala971Ala |
S95 |
3 | BAA03g42790 | A03 | 20247433 | C | T | missense_variant | MODERATE | c.2714G>A|p.Gly905Glu |
S299 |
4 | BAA03g42790 | A03 | 20247580 | G | A | missense_variant | MODERATE | c.2567C>T|p.Ser856Leu |
S130 |
5 | BAA03g42790 | A03 | 20247831 | G | A | synonymous_variant | LOW | c.2316C>T|p.Val772Val |
S282 |
6 | BAA03g42790 | A03 | 20247881 | C | T | missense_variant | MODERATE | c.2266G>A|p.Glu756Lys |
S132 S137 |
7 | BAA03g42790 | A03 | 20249454 | C | T | missense_variant | MODERATE | c.868G>A|p.Asp290Asn |
S15 |
8 | BAA03g42790 | A03 | 20249614 | C | T | synonymous_variant | LOW | c.708G>A|p.Glu236Glu |
S110 |
9 | BAA03g42790 | A03 | 20250203 | G | A | missense_variant | MODERATE | c.119C>T|p.Ala40Val |
S80 |
10 | BAA03g42790 | A03 | 20250206 | G | A | missense_variant | MODERATE | c.116C>T|p.Pro39Leu |
S178 |
11 | BAA03g42790 | A03 | 20252324 | C | T | upstream_gene_variant | MODIFIER | c.-2003G>A| |
S129 |
12 | BAA03g42790 | A03 | 20252394 | C | T | upstream_gene_variant | MODIFIER | c.-2073G>A| |
S136 |
13 | BAA03g42790 | A03 | 20252571 | G | A | upstream_gene_variant | MODIFIER | c.-2250C>T| |
S199 |
14 | BAA03g42790 | A03 | 20253409 | G | A | upstream_gene_variant | MODIFIER | c.-3088C>T| |
S10 |
15 | BAA03g42790 | A03 | 20254337 | C | T | upstream_gene_variant | MODIFIER | c.-4016G>A| |
S188 |