Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
5851 | BAA01g04810 | A01 | 2140569 | G | A | synonymous_variant | LOW | c.1851C>T|p.Phe617Phe |
S40 |
5852 | BAA01g04810 | A01 | 2141143 | C | T | synonymous_variant | LOW | c.1599G>A|p.Ser533Ser |
S166 |
5853 | BAA01g04790 | A01 | 2141338 | C | T | upstream_gene_variant | MODIFIER | c.-4091G>A| |
S46 |
5854 | BAA01g04810 | A01 | 2141609 | C | T | splice_region_variant&intron_variant | LOW | c.1377+8G>A| |
S267 |
5855 | BAA01g04810 | A01 | 2142187 | G | A | synonymous_variant | LOW | c.1056C>T|p.Leu352Leu |
S236 |
5856 | BAA01g04810 | A01 | 2144540 | G | A | upstream_gene_variant | MODIFIER | c.-16C>T| |
S174 |
5857 | BAA01g04820 | A01 | 2145140 | G | A | missense_variant | MODERATE | c.37G>A|p.Glu13Lys |
S241 |
5858 | BAA01g04810 | A01 | 2145750 | G | A | upstream_gene_variant | MODIFIER | c.-1226C>T| |
S183 S198 |
5859 | BAA01g04830 | A01 | 2150260 | C | T | upstream_gene_variant | MODIFIER | c.-1183C>T| |
S128 |
5860 | BAA01g04830 | A01 | 2150407 | C | T | upstream_gene_variant | MODIFIER | c.-1036C>T| |
S270 |
5861 | BAA01g04840 | A01 | 2151682 | C | T | downstream_gene_variant | MODIFIER | c.*1274G>A| |
S231 |
5862 | BAA01g04840 | A01 | 2152527 | G | A | downstream_gene_variant | MODIFIER | c.*429C>T| |
S45 |
5863 | BAA01g04830 | A01 | 2152651 | G | A | missense_variant | MODERATE | c.575G>A|p.Arg192His |
S80 |
5864 | BAA01g04840 | A01 | 2153102 | G | A | missense_variant | MODERATE | c.2254C>T|p.Arg752Cys |
S10 |
5865 | BAA01g04840 | A01 | 2153241 | C | T | synonymous_variant | LOW | c.2115G>A|p.Glu705Glu |
S192 |
5866 | BAA01g04830 | A01 | 2154296 | G | A | downstream_gene_variant | MODIFIER | c.*1626G>A| |
S259 |
5867 | BAA01g04840 | A01 | 2154996 | C | T | stop_gained | HIGH | c.1232G>A|p.Trp411* |
S282 |
5868 | BAA01g04830 | A01 | 2156642 | G | A | downstream_gene_variant | MODIFIER | c.*3972G>A| |
S96 |
5869 | BAA01g04840 | A01 | 2157789 | C | T | missense_variant | MODERATE | c.205G>A|p.Glu69Lys |
S182 |
5870 | BAA01g04840 | A01 | 2158625 | C | T | upstream_gene_variant | MODIFIER | c.-355G>A| |
S59 |
5871 | BAA01g04850 | A01 | 2159379 | C | T | missense_variant | MODERATE | c.53G>A|p.Arg18Gln |
S192 |
5872 | BAA01g04860 | A01 | 2160639 | G | A | missense_variant&splice_region_variant | MODERATE | c.470C>T|p.Ser157Phe |
S156 |
5873 | BAA01g04860 | A01 | 2161109 | C | T | missense_variant | MODERATE | c.236G>A|p.Arg79Lys |
S296 |
5874 | BAA01g04870 | A01 | 2162849 | C | T | synonymous_variant | LOW | c.618G>A|p.Lys206Lys |
S164 |
5875 | BAA01g04870 | A01 | 2163804 | C | T | missense_variant | MODERATE | c.301G>A|p.Glu101Lys |
S208 S93 |