Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21430 | A01 | 10632709 | C | T | missense_variant | MODERATE | c.2170G>A|p.Glu724Lys |
S269 |
2 | BAA01g21430 | A01 | 10633574 | G | A | splice_region_variant&intron_variant | LOW | c.1518-6C>T| |
S157 |
3 | BAA01g21430 | A01 | 10634810 | C | T | missense_variant | MODERATE | c.770G>A|p.Gly257Glu |
S171 |
4 | BAA01g21430 | A01 | 10635191 | C | T | missense_variant | MODERATE | c.488G>A|p.Gly163Glu |
S17 |
5 | BAA01g21430 | A01 | 10635534 | C | T | missense_variant | MODERATE | c.145G>A|p.Asp49Asn |
S189 |
6 | BAA01g21430 | A01 | 10635540 | C | T | missense_variant | MODERATE | c.139G>A|p.Glu47Lys |
S100 |
7 | BAA01g21430 | A01 | 10636453 | C | T | upstream_gene_variant | MODIFIER | c.-775G>A| |
S124 S126 S149 S176 S223 S255 S286 S287 S57 S61 |
8 | BAA01g21430 | A01 | 10636499 | C | T | upstream_gene_variant | MODIFIER | c.-821G>A| |
S183 |
9 | BAA01g21430 | A01 | 10637367 | G | A | upstream_gene_variant | MODIFIER | c.-1689C>T| |
S199 |
10 | BAA01g21430 | A01 | 10637454 | G | A | upstream_gene_variant | MODIFIER | c.-1776C>T| |
S28 |
11 | BAA01g21430 | A01 | 10637492 | C | T | upstream_gene_variant | MODIFIER | c.-1814G>A| |
S153 |
12 | BAA01g21430 | A01 | 10637510 | G | A | upstream_gene_variant | MODIFIER | c.-1832C>T| |
S45 |
13 | BAA01g21430 | A01 | 10637587 | G | A | upstream_gene_variant | MODIFIER | c.-1909C>T| |
S116 |
14 | BAA01g21430 | A01 | 10637592 | G | A | upstream_gene_variant | MODIFIER | c.-1914C>T| |
S159 S243 |
15 | BAA01g21430 | A01 | 10637746 | C | T | upstream_gene_variant | MODIFIER | c.-2068G>A| |
S289 S290 |