Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22060 | A10 | 19144463 | G | A | upstream_gene_variant | MODIFIER | c.-4500G>A| |
S298 |
2 | BAA10g22060 | A10 | 19145018 | C | T | upstream_gene_variant | MODIFIER | c.-3945C>T| |
S211 |
3 | BAA10g22060 | A10 | 19148087 | G | A | upstream_gene_variant | MODIFIER | c.-876G>A| |
S82 S92 |
4 | BAA10g22060 | A10 | 19148391 | G | T | upstream_gene_variant | MODIFIER | c.-572G>T| |
S104 S108 S12 S134 S146 S169 S176 S184 S192 S196 S238 S257 S279 S301 S68 |
5 | BAA10g22060 | A10 | 19149023 | G | A | intron_variant | MODIFIER | c.30+31G>A| |
S28 |
6 | BAA10g22060 | A10 | 19149188 | G | A | missense_variant | MODERATE | c.146G>A|p.Cys49Tyr |
S36 |
7 | BAA10g22060 | A10 | 19149252 | C | T | synonymous_variant | LOW | c.210C>T|p.Asn70Asn |
S10 |
8 | BAA10g22060 | A10 | 19149594 | G | A | synonymous_variant | LOW | c.552G>A|p.Arg184Arg |
S82 |
9 | BAA10g22060 | A10 | 19149621 | G | A | synonymous_variant | LOW | c.579G>A|p.Arg193Arg |
S168 S219 S72 |
10 | BAA10g22060 | A10 | 19149987 | G | A | downstream_gene_variant | MODIFIER | c.*345G>A| |
S160 |
11 | BAA10g22060 | A10 | 19154021 | C | T | downstream_gene_variant | MODIFIER | c.*4379C>T| |
S45 |