Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07560 | A10 | 4517269 | T | C | missense_variant | MODERATE | c.983A>G|p.Glu328Gly |
S303 |
2 | BAA10g07560 | A10 | 4518236 | C | T | missense_variant | MODERATE | c.652G>A|p.Gly218Ser |
S54 |
3 | BAA10g07560 | A10 | 4518473 | C | T | missense_variant | MODERATE | c.415G>A|p.Glu139Lys |
S271 |
4 | BAA10g07560 | A10 | 4520747 | C | T | upstream_gene_variant | MODIFIER | c.-1860G>A| |
S177 |
5 | BAA10g07560 | A10 | 4521095 | C | T | upstream_gene_variant | MODIFIER | c.-2208G>A| |
S177 |
6 | BAA10g07560 | A10 | 4521398 | T | G | upstream_gene_variant | MODIFIER | c.-2511A>C| |
S127 S162 S206 S62 |
7 | BAA10g07560 | A10 | 4521405 | C | T | upstream_gene_variant | MODIFIER | c.-2518G>A| |
S10 |
8 | BAA10g07560 | A10 | 4521653 | G | A | upstream_gene_variant | MODIFIER | c.-2766C>T| |
S157 S166 S167 S262 |
9 | BAA10g07560 | A10 | 4522021 | G | A | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S1 S90 |
10 | BAA10g07560 | A10 | 4522597 | C | T | upstream_gene_variant | MODIFIER | c.-3710G>A| |
S142 |
11 | BAA10g07560 | A10 | 4522680 | C | T | upstream_gene_variant | MODIFIER | c.-3793G>A| |
S92 |
12 | BAA10g07560 | A10 | 4522836 | G | A | upstream_gene_variant | MODIFIER | c.-3949C>T| |
S198 |
13 | BAA10g07560 | A10 | 4523176 | G | A | upstream_gene_variant | MODIFIER | c.-4289C>T| |
S274 |
14 | BAA10g07560 | A10 | 4523356 | C | T | upstream_gene_variant | MODIFIER | c.-4469G>A| |
S25 |
15 | BAA10g07560 | A10 | 4523460 | G | A | upstream_gene_variant | MODIFIER | c.-4573C>T| |
S189 |
16 | BAA10g07560 | A10 | 4523479 | G | A | upstream_gene_variant | MODIFIER | c.-4592C>T| |
S230 |