Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g18990 | A04 | 22620341 | G | A | missense_variant | MODERATE | c.4334C>T|p.Thr1445Ile |
S166 |
2 | BAA04g18990 | A04 | 22620358 | G | A | synonymous_variant | LOW | c.4317C>T|p.Arg1439Arg |
S245 |
3 | BAA04g18990 | A04 | 22620586 | C | T | intron_variant | MODIFIER | c.4161+29G>A| |
S197 |
4 | BAA04g18990 | A04 | 22620627 | C | T | synonymous_variant | LOW | c.4149G>A|p.Lys1383Lys |
S50 |
5 | BAA04g18990 | A04 | 22620937 | C | T | missense_variant | MODERATE | c.3839G>A|p.Arg1280Lys |
S28 |
6 | BAA04g18990 | A04 | 22621416 | C | T | synonymous_variant | LOW | c.3360G>A|p.Arg1120Arg |
S178 |
7 | BAA04g18990 | A04 | 22622213 | C | T | intron_variant | MODIFIER | c.2803-9G>A| |
S8 |
8 | BAA04g18990 | A04 | 22622442 | G | A | missense_variant | MODERATE | c.2651C>T|p.Ser884Phe |
S136 |
9 | BAA04g18990 | A04 | 22622987 | G | A | synonymous_variant | LOW | c.2106C>T|p.Asp702Asp |
S278 |
10 | BAA04g18990 | A04 | 22623578 | C | T | missense_variant | MODERATE | c.1726G>A|p.Glu576Lys |
S48 |
11 | BAA04g18990 | A04 | 22623904 | C | T | missense_variant | MODERATE | c.1400G>A|p.Ser467Asn |
S130 |
12 | BAA04g18990 | A04 | 22624528 | C | T | synonymous_variant | LOW | c.912G>A|p.Ser304Ser |
S53 S93 |
13 | BAA04g18990 | A04 | 22624629 | C | T | missense_variant | MODERATE | c.811G>A|p.Val271Met |
S28 |
14 | BAA04g18990 | A04 | 22624893 | C | T | missense_variant | MODERATE | c.547G>A|p.Gly183Arg |
S192 |
15 | BAA04g18990 | A04 | 22624913 | C | T | missense_variant | MODERATE | c.527G>A|p.Ser176Asn |
S172 |
16 | BAA04g18990 | A04 | 22625132 | G | A | missense_variant | MODERATE | c.308C>T|p.Pro103Leu |
S36 |
17 | BAA04g18990 | A04 | 22625189 | G | A | missense_variant | MODERATE | c.251C>T|p.Ala84Val |
S60 |
18 | BAA04g18990 | A04 | 22625285 | C | T | missense_variant | MODERATE | c.155G>A|p.Gly52Glu |
S297 |
19 | BAA04g18990 | A04 | 22626203 | C | T | upstream_gene_variant | MODIFIER | c.-764G>A| |
S8 |
20 | BAA04g18990 | A04 | 22627022 | C | T | upstream_gene_variant | MODIFIER | c.-1583G>A| |
S216 S241 |
21 | BAA04g18990 | A04 | 22627896 | G | A | upstream_gene_variant | MODIFIER | c.-2457C>T| |
S183 S198 |
22 | BAA04g18990 | A04 | 22630272 | G | A | upstream_gene_variant | MODIFIER | c.-4833C>T| |
S286 |