Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13350 | A01 | 6323484 | G | A | missense_variant | MODERATE | c.22G>A|p.Glu8Lys |
S60 |
2 | BAA01g13350 | A01 | 6324133 | G | A | synonymous_variant | LOW | c.300G>A|p.Leu100Leu |
S240 |
3 | BAA01g13350 | A01 | 6324307 | G | A | missense_variant | MODERATE | c.388G>A|p.Glu130Lys |
S180 |
4 | BAA01g13350 | A01 | 6324429 | C | T | synonymous_variant | LOW | c.510C>T|p.Ala170Ala |
S20 |
5 | BAA01g13350 | A01 | 6325692 | C | T | missense_variant | MODERATE | c.1052C>T|p.Pro351Leu |
S99 |
6 | BAA01g13350 | A01 | 6326853 | G | A | missense_variant | MODERATE | c.1612G>A|p.Glu538Lys |
S161 |
7 | BAA01g13350 | A01 | 6327280 | C | T | missense_variant | MODERATE | c.1745C>T|p.Thr582Ile |
S296 |
8 | BAA01g13350 | A01 | 6327900 | C | T | missense_variant | MODERATE | c.2108C>T|p.Thr703Ile |
S213 |
9 | BAA01g13350 | A01 | 6328348 | G | A | missense_variant | MODERATE | c.2308G>A|p.Glu770Lys |
S273 |
10 | BAA01g13350 | A01 | 6329517 | G | A | downstream_gene_variant | MODIFIER | c.*1149G>A| |
S110 |
11 | BAA01g13350 | A01 | 6329605 | C | T | downstream_gene_variant | MODIFIER | c.*1237C>T| |
S223 |
12 | BAA01g13350 | A01 | 6329665 | C | T | downstream_gene_variant | MODIFIER | c.*1297C>T| |
S169 |
13 | BAA01g13350 | A01 | 6329803 | G | A | downstream_gene_variant | MODIFIER | c.*1435G>A| |
S175 |
14 | BAA01g13350 | A01 | 6333127 | G | A | downstream_gene_variant | MODIFIER | c.*4759G>A| |
S298 |
15 | BAA01g13350 | A01 | 6333268 | G | A | downstream_gene_variant | MODIFIER | c.*4900G>A| |
S12 |