Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11130 | A10 | 12785999 | G | C | upstream_gene_variant | MODIFIER | c.-4827G>C| |
|
2 | BAA10g11130 | A10 | 12786007 | G | A | upstream_gene_variant | MODIFIER | c.-4819G>A| |
S18 |
3 | BAA10g11130 | A10 | 12786058 | C | T | upstream_gene_variant | MODIFIER | c.-4768C>T| |
S199 |
4 | BAA10g11130 | A10 | 12786177 | G | A | upstream_gene_variant | MODIFIER | c.-4649G>A| |
S176 |
5 | BAA10g11130 | A10 | 12786325 | G | A | upstream_gene_variant | MODIFIER | c.-4501G>A| |
S219 S72 |
6 | BAA10g11130 | A10 | 12786590 | G | A | upstream_gene_variant | MODIFIER | c.-4236G>A| |
S71 |
7 | BAA10g11130 | A10 | 12790845 | G | A | missense_variant | MODERATE | c.20G>A|p.Gly7Asp |
S296 |
8 | BAA10g11130 | A10 | 12790977 | C | T | missense_variant | MODERATE | c.152C>T|p.Pro51Leu |
S287 |
9 | BAA10g11130 | A10 | 12791920 | G | A | missense_variant | MODERATE | c.895G>A|p.Asp299Asn |
S100 |
10 | BAA10g11130 | A10 | 12792079 | C | T | synonymous_variant | LOW | c.1054C>T|p.Leu352Leu |
S252 |
11 | BAA10g11130 | A10 | 12794258 | G | A | downstream_gene_variant | MODIFIER | c.*2159G>A| |
S136 |
12 | BAA10g11130 | A10 | 12794322 | C | T | downstream_gene_variant | MODIFIER | c.*2223C>T| |
S46 |
13 | BAA10g11130 | A10 | 12795783 | C | T | downstream_gene_variant | MODIFIER | c.*3684C>T| |
S191 |