Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g22440 | A05 | 26979022 | G | A | missense_variant | MODERATE | c.2230C>T|p.Pro744Ser |
S41 |
2 | BAA05g22440 | A05 | 26979676 | C | T | missense_variant | MODERATE | c.1663G>A|p.Asp555Asn |
S177 |
3 | BAA05g22440 | A05 | 26979769 | C | T | missense_variant | MODERATE | c.1570G>A|p.Gly524Arg |
S28 |
4 | BAA05g22440 | A05 | 26981782 | G | A | missense_variant | MODERATE | c.641C>T|p.Ala214Val |
S184 |
5 | BAA05g22440 | A05 | 26982362 | C | T | missense_variant | MODERATE | c.266G>A|p.Arg89Lys |
S239 S33 |
6 | BAA05g22440 | A05 | 26982966 | G | A | upstream_gene_variant | MODIFIER | c.-339C>T| |
S163 |
7 | BAA05g22440 | A05 | 26984489 | T | A | upstream_gene_variant | MODIFIER | c.-1862A>T| |
S11 S207 S40 S49 S71 |
8 | BAA05g22440 | A05 | 26985295 | G | A | upstream_gene_variant | MODIFIER | c.-2668C>T| |
S275 |
9 | BAA05g22440 | A05 | 26985411 | C | T | upstream_gene_variant | MODIFIER | c.-2784G>A| |
S269 |
10 | BAA05g22440 | A05 | 26985767 | C | T | upstream_gene_variant | MODIFIER | c.-3140G>A| |
S74 |
11 | BAA05g22440 | A05 | 26986528 | C | T | upstream_gene_variant | MODIFIER | c.-3901G>A| |
S188 |
12 | BAA05g22440 | A05 | 26986711 | C | T | upstream_gene_variant | MODIFIER | c.-4084G>A| |
S192 |
13 | BAA05g22440 | A05 | 26986723 | C | T | upstream_gene_variant | MODIFIER | c.-4096G>A| |
S130 |
14 | BAA05g22440 | A05 | 26987254 | G | A | upstream_gene_variant | MODIFIER | c.-4627C>T| |
S238 |
15 | BAA05g22440 | A05 | 26987314 | G | A | upstream_gene_variant | MODIFIER | c.-4687C>T| |
S165 |
16 | BAA05g22440 | A05 | 26987440 | C | T | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S148 S30 S31 |
17 | BAA05g22440 | A05 | 26987519 | A | G | upstream_gene_variant | MODIFIER | c.-4892T>C| |
S1 S90 |