Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42970 | A05 | 40514840 | C | T | missense_variant | MODERATE | c.2482G>A|p.Glu828Lys |
S155 S211 |
2 | BAA05g42970 | A05 | 40515416 | C | T | missense_variant | MODERATE | c.2059G>A|p.Glu687Lys |
S150 |
3 | BAA05g42970 | A05 | 40515578 | G | A | missense_variant | MODERATE | c.1897C>T|p.Arg633Cys |
S35 |
4 | BAA05g42970 | A05 | 40515652 | C | T | missense_variant | MODERATE | c.1823G>A|p.Ser608Asn |
S279 |
5 | BAA05g42970 | A05 | 40515929 | C | T | missense_variant | MODERATE | c.1546G>A|p.Glu516Lys |
S250 |
6 | BAA05g42970 | A05 | 40516047 | G | A | synonymous_variant | LOW | c.1428C>T|p.Leu476Leu |
S166 |
7 | BAA05g42970 | A05 | 40516100 | C | T | missense_variant | MODERATE | c.1375G>A|p.Glu459Lys |
S271 |
8 | BAA05g42970 | A05 | 40516662 | G | A | synonymous_variant | LOW | c.813C>T|p.Leu271Leu |
S72 S78 |
9 | BAA05g42970 | A05 | 40517111 | G | A | synonymous_variant | LOW | c.603C>T|p.Ser201Ser |
S121 |
10 | BAA05g42970 | A05 | 40518176 | G | A | missense_variant | MODERATE | c.169C>T|p.Pro57Ser |
S292 |
11 | BAA05g42970 | A05 | 40519705 | T | C | upstream_gene_variant | MODIFIER | c.-605A>G| |
S306 S308 |
12 | BAA05g42970 | A05 | 40521462 | C | T | upstream_gene_variant | MODIFIER | c.-2362G>A| |
S179 |
13 | BAA05g42970 | A05 | 40521764 | T | C | upstream_gene_variant | MODIFIER | c.-2664A>G| |
S157 S163 |
14 | BAA05g42970 | A05 | 40523298 | G | A | upstream_gene_variant | MODIFIER | c.-4198C>T| |
S8 |
15 | BAA05g42970 | A05 | 40523509 | C | T | upstream_gene_variant | MODIFIER | c.-4409G>A| |
S156 |