Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2151 | BAA01g01730 | A01 | 774760 | C | T | upstream_gene_variant | MODIFIER | c.-3578C>T| |
S206 S26 |
2152 | BAA01g01720 | A01 | 775618 | G | A | missense_variant | MODERATE | c.955G>A|p.Val319Ile |
S295 |
2153 | BAA01g01720 | A01 | 775672 | G | A | missense_variant | MODERATE | c.1009G>A|p.Val337Ile |
S15 S3 |
2154 | BAA01g01720 | A01 | 775759 | C | T | synonymous_variant | LOW | c.1096C>T|p.Leu366Leu |
S38 |
2155 | BAA01g01730 | A01 | 776715 | C | T | upstream_gene_variant | MODIFIER | c.-1623C>T| |
S244 |
2156 | BAA01g01730 | A01 | 777659 | C | T | upstream_gene_variant | MODIFIER | c.-679C>T| |
S276 |
2157 | BAA01g01730 | A01 | 777836 | G | A | upstream_gene_variant | MODIFIER | c.-502G>A| |
S293 |
2158 | BAA01g01730 | A01 | 778745 | C | T | synonymous_variant | LOW | c.408C>T|p.Val136Val |
S278 |
2159 | BAA01g01730 | A01 | 779642 | C | T | missense_variant | MODERATE | c.662C>T|p.Ser221Leu |
S208 S219 |
2160 | BAA01g01730 | A01 | 780488 | G | A | missense_variant | MODERATE | c.1109G>A|p.Arg370Lys |
S202 |
2161 | BAA01g01740 | A01 | 783915 | C | T | upstream_gene_variant | MODIFIER | c.-684G>A| |
S150 |
2162 | BAA01g01770-BAA01g01780 | A01 | 803416 | C | T | intergenic_region | MODIFIER | n.803416C>T| |
S25 |
2163 | BAA01g01770-BAA01g01780 | A01 | 804232 | G | A | intergenic_region | MODIFIER | n.804232G>A| |
S149 |
2164 | BAA01g01770-BAA01g01780 | A01 | 804932 | C | T | intergenic_region | MODIFIER | n.804932C>T| |
S208 |
2165 | BAA01g01770-BAA01g01780 | A01 | 805455 | G | A | intergenic_region | MODIFIER | n.805455G>A| |
S279 |
2166 | BAA01g01770-BAA01g01780 | A01 | 807058 | C | T | intergenic_region | MODIFIER | n.807058C>T| |
S266 |
2167 | BAA01g01780 | A01 | 809914 | G | A | upstream_gene_variant | MODIFIER | c.-2630G>A| |
S33 |
2168 | BAA01g01780 | A01 | 811083 | G | A | upstream_gene_variant | MODIFIER | c.-1461G>A| |
S103 |
2169 | BAA01g01780 | A01 | 811112 | G | A | upstream_gene_variant | MODIFIER | c.-1432G>A| |
S262 |
2170 | BAA01g01780 | A01 | 811419 | G | A | upstream_gene_variant | MODIFIER | c.-1125G>A| |
S162 |
2171 | BAA01g01780 | A01 | 812923 | C | T | missense_variant | MODERATE | c.380C>T|p.Ser127Phe |
S18 |
2172 | BAA01g01780 | A01 | 813839 | G | A | synonymous_variant | LOW | c.1296G>A|p.Glu432Glu |
S6 |
2173 | BAA01g01780 | A01 | 813935 | G | A | synonymous_variant | LOW | c.1392G>A|p.Ala464Ala |
S32 |
2174 | BAA01g01780 | A01 | 814479 | G | A | synonymous_variant | LOW | c.1839G>A|p.Arg613Arg |
S17 |
2175 | BAA01g01790 | A01 | 817565 | G | A | upstream_gene_variant | MODIFIER | c.-99C>T| |
S11 |