Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19000 | A10 | 17595019 | G | A | upstream_gene_variant | MODIFIER | c.-1211G>A| |
S184 |
2 | BAA10g19000 | A10 | 17595027 | G | A | upstream_gene_variant | MODIFIER | c.-1203G>A| |
S36 |
3 | BAA10g19000 | A10 | 17595897 | C | T | upstream_gene_variant | MODIFIER | c.-333C>T| |
S123 |
4 | BAA10g19000 | A10 | 17598022 | C | T | synonymous_variant | LOW | c.573C>T|p.Phe191Phe |
S70 |
5 | BAA10g19000 | A10 | 17598340 | C | T | missense_variant | MODERATE | c.821C>T|p.Ala274Val |
S23 |
6 | BAA10g19000 | A10 | 17598348 | G | A | missense_variant&splice_region_variant | MODERATE | c.829G>A|p.Glu277Lys |
S251 |
7 | BAA10g19000 | A10 | 17599909 | G | A | missense_variant | MODERATE | c.1444G>A|p.Ala482Thr |
S74 |
8 | BAA10g19000 | A10 | 17600384 | G | A | downstream_gene_variant | MODIFIER | c.*440G>A| |
S126 |
9 | BAA10g19000 | A10 | 17600896 | C | T | downstream_gene_variant | MODIFIER | c.*952C>T| |
S20 |