Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g09080 | A04 | 6375329 | G | A | missense_variant | MODERATE | c.1445C>T|p.Thr482Ile |
S295 |
2 | BAA04g09080 | A04 | 6375351 | G | A | missense_variant | MODERATE | c.1423C>T|p.Pro475Ser |
S162 |
3 | BAA04g09080 | A04 | 6376099 | G | A | intron_variant | MODIFIER | c.739-64C>T| |
S282 |
4 | BAA04g09080 | A04 | 6376229 | G | A | missense_variant | MODERATE | c.734C>T|p.Ser245Phe |
S16 |
5 | BAA04g09080 | A04 | 6376493 | C | T | missense_variant | MODERATE | c.470G>A|p.Arg157Lys |
S70 |
6 | BAA04g09080 | A04 | 6376538 | C | T | missense_variant | MODERATE | c.425G>A|p.Arg142Lys |
S265 |
7 | BAA04g09080 | A04 | 6376626 | C | T | missense_variant | MODERATE | c.337G>A|p.Asp113Asn |
S63 |
8 | BAA04g09080 | A04 | 6376629 | G | A | missense_variant | MODERATE | c.334C>T|p.Pro112Ser |
S114 |
9 | BAA04g09080 | A04 | 6376848 | C | T | missense_variant | MODERATE | c.115G>A|p.Asp39Asn |
S186 S275 |
10 | BAA04g09080 | A04 | 6377317 | C | T | upstream_gene_variant | MODIFIER | c.-355G>A| |
S25 |
11 | BAA04g09080 | A04 | 6377578 | C | T | upstream_gene_variant | MODIFIER | c.-616G>A| |
S283 |
12 | BAA04g09080 | A04 | 6377589 | G | A | upstream_gene_variant | MODIFIER | c.-627C>T| |
S66 |
13 | BAA04g09080 | A04 | 6377646 | C | T | upstream_gene_variant | MODIFIER | c.-684G>A| |
S293 |
14 | BAA04g09080 | A04 | 6378897 | C | T | upstream_gene_variant | MODIFIER | c.-1935G>A| |
S284 |
15 | BAA04g09080 | A04 | 6380905 | G | A | upstream_gene_variant | MODIFIER | c.-3943C>T| |
S169 |
16 | BAA04g09080 | A04 | 6381420 | G | A | upstream_gene_variant | MODIFIER | c.-4458C>T| |
S246 S303 |
17 | BAA04g09080 | A04 | 6381894 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S130 S171 |