Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10600 | A10 | 12334384 | G | A | upstream_gene_variant | MODIFIER | c.-4615G>A| |
S292 |
2 | BAA10g10600 | A10 | 12334685 | C | T | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S199 |
3 | BAA10g10600 | A10 | 12335080 | C | T | upstream_gene_variant | MODIFIER | c.-3919C>T| |
S2 |
4 | BAA10g10600 | A10 | 12335222 | G | A | upstream_gene_variant | MODIFIER | c.-3777G>A| |
S43 |
5 | BAA10g10600 | A10 | 12335515 | G | A | upstream_gene_variant | MODIFIER | c.-3484G>A| |
S279 |
6 | BAA10g10600 | A10 | 12337409 | G | A | upstream_gene_variant | MODIFIER | c.-1590G>A| |
S67 |
7 | BAA10g10600 | A10 | 12338186 | C | T | upstream_gene_variant | MODIFIER | c.-813C>T| |
S133 |
8 | BAA10g10600 | A10 | 12339995 | G | A | missense_variant | MODERATE | c.487G>A|p.Glu163Lys |
S245 |
9 | BAA10g10600 | A10 | 12340956 | G | A | missense_variant | MODERATE | c.1145G>A|p.Arg382Lys |
S172 |
10 | BAA10g10600 | A10 | 12341056 | G | A | synonymous_variant | LOW | c.1245G>A|p.Thr415Thr |
S209 |
11 | BAA10g10600 | A10 | 12343151 | G | A | downstream_gene_variant | MODIFIER | c.*1451G>A| |
S161 |
12 | BAA10g10600 | A10 | 12343184 | C | T | downstream_gene_variant | MODIFIER | c.*1484C>T| |
S80 |
13 | BAA10g10600 | A10 | 12344278 | C | T | downstream_gene_variant | MODIFIER | c.*2578C>T| |
S33 |
14 | BAA10g10600 | A10 | 12345976 | C | T | downstream_gene_variant | MODIFIER | c.*4276C>T| |
S54 |
15 | BAA10g10600 | A10 | 12346309 | G | A | downstream_gene_variant | MODIFIER | c.*4609G>A| |
S125 |
16 | BAA10g10600 | A10 | 12346424 | C | T | downstream_gene_variant | MODIFIER | c.*4724C>T| |
S143 |