Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07840 | A05 | 3938454 | C | T | missense_variant | MODERATE | c.3010G>A|p.Val1004Ile |
S185 |
2 | BAA05g07840 | A05 | 3939159 | G | A | missense_variant | MODERATE | c.2500C>T|p.His834Tyr |
S247 |
3 | BAA05g07840 | A05 | 3939173 | G | A | missense_variant | MODERATE | c.2486C>T|p.Thr829Ile |
S178 |
4 | BAA05g07840 | A05 | 3941104 | C | T | missense_variant | MODERATE | c.1753G>A|p.Ala585Thr |
S202 |
5 | BAA05g07840 | A05 | 3941245 | C | T | missense_variant | MODERATE | c.1612G>A|p.Glu538Lys |
S9 |
6 | BAA05g07840 | A05 | 3941967 | C | T | synonymous_variant | LOW | c.1041G>A|p.Lys347Lys |
S5 |
7 | BAA05g07840 | A05 | 3941980 | C | T | missense_variant | MODERATE | c.1028G>A|p.Arg343Lys |
S292 |
8 | BAA05g07840 | A05 | 3943328 | C | T | missense_variant | MODERATE | c.357G>A|p.Met119Ile |
S52 |
9 | BAA05g07840 | A05 | 3943884 | C | T | upstream_gene_variant | MODIFIER | c.-121G>A| |
S25 |
10 | BAA05g07840 | A05 | 3943968 | G | A | upstream_gene_variant | MODIFIER | c.-205C>T| |
S245 |
11 | BAA05g07840 | A05 | 3944231 | G | A | upstream_gene_variant | MODIFIER | c.-468C>T| |
S15 S3 |
12 | BAA05g07840 | A05 | 3944258 | C | T | upstream_gene_variant | MODIFIER | c.-495G>A| |
S265 |
13 | BAA05g07840 | A05 | 3945403 | G | A | upstream_gene_variant | MODIFIER | c.-1640C>T| |
S186 |
14 | BAA05g07840 | A05 | 3948141 | G | A | upstream_gene_variant | MODIFIER | c.-4378C>T| |
S298 |
15 | BAA05g07840 | A05 | 3948166 | G | A | upstream_gene_variant | MODIFIER | c.-4403C>T| |
S77 S82 |