Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g29470 | A09 | 19707549 | G | T | stop_gained | HIGH | c.76G>T|p.Gly26* |
S36 |
2 | BAA09g29470 | A09 | 19707588 | G | A | missense_variant | MODERATE | c.115G>A|p.Asp39Asn |
S185 |
3 | BAA09g29470 | A09 | 19707702 | C | T | synonymous_variant | LOW | c.229C>T|p.Leu77Leu |
S293 |
4 | BAA09g29470 | A09 | 19707865 | C | T | missense_variant | MODERATE | c.392C>T|p.Ser131Leu |
S289 S290 |
5 | BAA09g29470 | A09 | 19708167 | G | A | missense_variant | MODERATE | c.694G>A|p.Ala232Thr |
S155 S211 |
6 | BAA09g29470 | A09 | 19708232 | G | A | synonymous_variant | LOW | c.759G>A|p.Glu253Glu |
S167 |
7 | BAA09g29470 | A09 | 19708467 | G | A | missense_variant | MODERATE | c.994G>A|p.Glu332Lys |
S79 S84 |
8 | BAA09g29470 | A09 | 19709298 | G | A | missense_variant | MODERATE | c.1579G>A|p.Ala527Thr |
S177 |
9 | BAA09g29470 | A09 | 19709999 | G | A | synonymous_variant | LOW | c.2280G>A|p.Leu760Leu |
S233 |
10 | BAA09g29470 | A09 | 19710019 | G | A | stop_gained | HIGH | c.2300G>A|p.Trp767* |
S47 |
11 | BAA09g29470 | A09 | 19712192 | G | A | downstream_gene_variant | MODIFIER | c.*1995G>A| |
S180 |
12 | BAA09g29470 | A09 | 19712472 | C | T | downstream_gene_variant | MODIFIER | c.*2275C>T| |
S88 |
13 | BAA09g29470 | A09 | 19712667 | C | T | downstream_gene_variant | MODIFIER | c.*2470C>T| |
S208 |
14 | BAA09g29470 | A09 | 19713344 | G | A | downstream_gene_variant | MODIFIER | c.*3147G>A| |
S132 S137 S215 |
15 | BAA09g29470 | A09 | 19713594 | G | A | downstream_gene_variant | MODIFIER | c.*3397G>A| |
S196 |
16 | BAA09g29470 | A09 | 19714067 | C | T | downstream_gene_variant | MODIFIER | c.*3870C>T| |
S172 S217 |
17 | BAA09g29470 | A09 | 19714410 | T | A | downstream_gene_variant | MODIFIER | c.*4213T>A| |
S294 |
18 | BAA09g29470 | A09 | 19714511 | C | T | downstream_gene_variant | MODIFIER | c.*4314C>T| |
S257 |
19 | BAA09g29470 | A09 | 19714663 | G | T | downstream_gene_variant | MODIFIER | c.*4466G>T| |
S25 S264 |
20 | BAA09g29470 | A09 | 19714771 | C | T | downstream_gene_variant | MODIFIER | c.*4574C>T| |
S173 |