Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g26850 | A07 | 28856556 | C | T | missense_variant | MODERATE | c.6379G>A|p.Ala2127Thr |
S203 |
2 | BAA07g26850 | A07 | 28857277 | C | T | synonymous_variant | LOW | c.5811G>A|p.Leu1937Leu |
S99 |
3 | BAA07g26850 | A07 | 28857668 | C | T | missense_variant | MODERATE | c.5519G>A|p.Arg1840Lys |
S265 |
4 | BAA07g26850 | A07 | 28857775 | G | A | synonymous_variant | LOW | c.5412C>T|p.Ser1804Ser |
S130 |
5 | BAA07g26850 | A07 | 28857776 | G | A | missense_variant | MODERATE | c.5411C>T|p.Ser1804Phe |
S298 |
6 | BAA07g26850 | A07 | 28858000 | G | A | synonymous_variant | LOW | c.5187C>T|p.Leu1729Leu |
S278 |
7 | BAA07g26850 | A07 | 28858126 | C | T | synonymous_variant | LOW | c.5061G>A|p.Leu1687Leu |
S224 S279 |
8 | BAA07g26850 | A07 | 28858468 | G | A | synonymous_variant | LOW | c.4719C>T|p.Ile1573Ile |
S208 S219 |
9 | BAA07g26850 | A07 | 28858503 | G | A | synonymous_variant | LOW | c.4684C>T|p.Leu1562Leu |
S107 S11 |
10 | BAA07g26850 | A07 | 28858682 | C | T | missense_variant | MODERATE | c.4505G>A|p.Gly1502Glu |
S35 |
11 | BAA07g26850 | A07 | 28859013 | G | A | missense_variant | MODERATE | c.4174C>T|p.Pro1392Ser |
S115 |
12 | BAA07g26850 | A07 | 28859037 | G | A | missense_variant | MODERATE | c.4150C>T|p.Pro1384Ser |
S299 |
13 | BAA07g26850 | A07 | 28859959 | C | T | missense_variant | MODERATE | c.3228G>A|p.Met1076Ile |
S41 |
14 | BAA07g26850 | A07 | 28860797 | C | T | missense_variant | MODERATE | c.2717G>A|p.Gly906Glu |
S301 S304 |
15 | BAA07g26850 | A07 | 28860991 | C | T | synonymous_variant | LOW | c.2523G>A|p.Lys841Lys |
S109 |
16 | BAA07g26850 | A07 | 28861399 | G | A | synonymous_variant | LOW | c.2115C>T|p.Ser705Ser |
S65 |
17 | BAA07g26850 | A07 | 28861762 | G | A | synonymous_variant | LOW | c.1752C>T|p.Val584Val |
S189 |
18 | BAA07g26850 | A07 | 28862148 | G | A | missense_variant | MODERATE | c.1366C>T|p.Arg456Cys |
S130 |
19 | BAA07g26850 | A07 | 28862529 | C | T | missense_variant | MODERATE | c.985G>A|p.Ala329Thr |
S233 |
20 | BAA07g26850 | A07 | 28864465 | G | A | upstream_gene_variant | MODIFIER | c.-893C>T| |
S205 |
21 | BAA07g26850 | A07 | 28865335 | A | C | upstream_gene_variant | MODIFIER | c.-1763T>G| |
S80 |
22 | BAA07g26850 | A07 | 28865649 | C | T | upstream_gene_variant | MODIFIER | c.-2077G>A| |
S200 |
23 | BAA07g26850 | A07 | 28867629 | G | A | upstream_gene_variant | MODIFIER | c.-4057C>T| |
S115 |
24 | BAA07g26850 | A07 | 28868084 | C | T | upstream_gene_variant | MODIFIER | c.-4512G>A| |
S249 |