Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g28490 | A05 | 32373614 | G | A | missense_variant | MODERATE | c.5279C>T|p.Ser1760Leu |
S133 |
2 | BAA05g28490 | A05 | 32373709 | G | A | synonymous_variant | LOW | c.5184C>T|p.Ser1728Ser |
S11 |
3 | BAA05g28490 | A05 | 32374382 | G | A | missense_variant | MODERATE | c.4936C>T|p.Leu1646Phe |
S210 |
4 | BAA05g28490 | A05 | 32375042 | G | A | missense_variant | MODERATE | c.4621C>T|p.Arg1541Cys |
S267 |
5 | BAA05g28490 | A05 | 32376205 | C | T | missense_variant | MODERATE | c.3775G>A|p.Glu1259Lys |
S61 |
6 | BAA05g28490 | A05 | 32377132 | C | T | missense_variant | MODERATE | c.2848G>A|p.Gly950Arg |
S157 |
7 | BAA05g28490 | A05 | 32377213 | G | A | synonymous_variant | LOW | c.2767C>T|p.Leu923Leu |
S35 |
8 | BAA05g28490 | A05 | 32378092 | C | T | missense_variant | MODERATE | c.1888G>A|p.Asp630Asn |
S198 |
9 | BAA05g28490 | A05 | 32378349 | G | A | missense_variant | MODERATE | c.1631C>T|p.Ser544Phe |
S238 |
10 | BAA05g28490 | A05 | 32379432 | C | T | synonymous_variant | LOW | c.1050G>A|p.Thr350Thr |
S17 |
11 | BAA05g28490 | A05 | 32379943 | G | A | missense_variant | MODERATE | c.539C>T|p.Pro180Leu |
S257 |
12 | BAA05g28490 | A05 | 32381174 | G | A | upstream_gene_variant | MODIFIER | c.-577C>T| |
S85 |
13 | BAA05g28490 | A05 | 32381566 | C | T | upstream_gene_variant | MODIFIER | c.-969G>A| |
S250 |
14 | BAA05g28490 | A05 | 32382772 | C | T | upstream_gene_variant | MODIFIER | c.-2175G>A| |
S92 |
15 | BAA05g28490 | A05 | 32382869 | G | A | upstream_gene_variant | MODIFIER | c.-2272C>T| |
S67 |
16 | BAA05g28490 | A05 | 32382965 | G | A | upstream_gene_variant | MODIFIER | c.-2368C>T| |
S303 |
17 | BAA05g28490 | A05 | 32382968 | G | A | upstream_gene_variant | MODIFIER | c.-2371C>T| |
S38 |
18 | BAA05g28490 | A05 | 32383169 | C | T | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S115 |
19 | BAA05g28490 | A05 | 32384769 | C | T | upstream_gene_variant | MODIFIER | c.-4172G>A| |
S37 |
20 | BAA05g28490 | A05 | 32384983 | G | A | upstream_gene_variant | MODIFIER | c.-4386C>T| |
S231 |