Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g06950 | A05 | 3393867 | C | T | missense_variant | MODERATE | c.1685G>A|p.Gly562Glu |
S88 |
2 | BAA05g06950 | A05 | 3394682 | G | A | missense_variant | MODERATE | c.1325C>T|p.Pro442Leu |
S219 |
3 | BAA05g06950 | A05 | 3394819 | C | T | synonymous_variant | LOW | c.1188G>A|p.Arg396Arg |
S250 S59 |
4 | BAA05g06950 | A05 | 3395458 | G | A | missense_variant | MODERATE | c.701C>T|p.Thr234Ile |
S265 |
5 | BAA05g06950 | A05 | 3395476 | G | A | missense_variant | MODERATE | c.683C>T|p.Ser228Phe |
S40 S49 |
6 | BAA05g06950 | A05 | 3395918 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S166 |
7 | BAA05g06950 | A05 | 3396410 | C | T | intron_variant | MODIFIER | c.60+27G>A| |
S208 S93 |
8 | BAA05g06950 | A05 | 3396452 | G | A | synonymous_variant | LOW | c.45C>T|p.Asp15Asp |
S231 |
9 | BAA05g06950 | A05 | 3396550 | C | T | upstream_gene_variant | MODIFIER | c.-54G>A| |
S207 |
10 | BAA05g06950 | A05 | 3396729 | C | T | upstream_gene_variant | MODIFIER | c.-233G>A| |
S42 |
11 | BAA05g06950 | A05 | 3398443 | C | T | upstream_gene_variant | MODIFIER | c.-1947G>A| |
S267 |
12 | BAA05g06950 | A05 | 3398949 | T | C | upstream_gene_variant | MODIFIER | c.-2453A>G| |
S168 |
13 | BAA05g06950 | A05 | 3398954 | T | A | upstream_gene_variant | MODIFIER | c.-2458A>T| |
S168 |
14 | BAA05g06950 | A05 | 3399924 | G | A | upstream_gene_variant | MODIFIER | c.-3428C>T| |
S1 |
15 | BAA05g06950 | A05 | 3400327 | G | A | upstream_gene_variant | MODIFIER | c.-3831C>T| |
S279 |
16 | BAA05g06950 | A05 | 3400471 | G | T | upstream_gene_variant | MODIFIER | c.-3975C>A| |
S123 |