Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g25930 | A04 | 26757482 | C | T | missense_variant | MODERATE | c.1790G>A|p.Cys597Tyr |
S68 |
2 | BAA04g25930 | A04 | 26757575 | C | T | missense_variant | MODERATE | c.1697G>A|p.Arg566Lys |
S89 |
3 | BAA04g25930 | A04 | 26757588 | C | T | missense_variant | MODERATE | c.1684G>A|p.Asp562Asn |
S215 |
4 | BAA04g25930 | A04 | 26757721 | C | T | synonymous_variant | LOW | c.1551G>A|p.Glu517Glu |
S266 |
5 | BAA04g25930 | A04 | 26757805 | G | A | synonymous_variant | LOW | c.1467C>T|p.Tyr489Tyr |
S211 S227 |
6 | BAA04g25930 | A04 | 26758837 | G | A | intron_variant | MODIFIER | c.811-140C>T| |
S194 |
7 | BAA04g25930 | A04 | 26759150 | C | T | missense_variant | MODERATE | c.748G>A|p.Gly250Arg |
S67 |
8 | BAA04g25930 | A04 | 26759156 | C | T | missense_variant | MODERATE | c.742G>A|p.Glu248Lys |
S155 S211 |
9 | BAA04g25930 | A04 | 26759432 | C | T | missense_variant | MODERATE | c.466G>A|p.Gly156Arg |
S41 |
10 | BAA04g25930 | A04 | 26759660 | C | T | missense_variant | MODERATE | c.238G>A|p.Gly80Ser |
S217 |
11 | BAA04g25930 | A04 | 26759898 | C | T | upstream_gene_variant | MODIFIER | c.-1G>A| |
S2 |
12 | BAA04g25930 | A04 | 26760431 | C | T | upstream_gene_variant | MODIFIER | c.-534G>A| |
S204 |
13 | BAA04g25930 | A04 | 26760446 | C | T | upstream_gene_variant | MODIFIER | c.-549G>A| |
S135 |
14 | BAA04g25930 | A04 | 26762939 | G | A | upstream_gene_variant | MODIFIER | c.-3042C>T| |
S239 |
15 | BAA04g25930 | A04 | 26763576 | T | A | upstream_gene_variant | MODIFIER | c.-3679A>T| |
S249 |
16 | BAA04g25930 | A04 | 26764481 | C | T | upstream_gene_variant | MODIFIER | c.-4584G>A| |
S46 |