Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
6151 | BAA01g05100 | A01 | 2244786 | G | A | missense_variant | MODERATE | c.827G>A|p.Gly276Glu |
S63 |
6152 | BAA01g05100 | A01 | 2245075 | G | A | synonymous_variant | LOW | c.1116G>A|p.Glu372Glu |
S159 S243 |
6153 | BAA01g05100 | A01 | 2245123 | G | A | synonymous_variant | LOW | c.1164G>A|p.Lys388Lys |
S236 |
6154 | BAA01g05100 | A01 | 2245196 | C | T | splice_region_variant&intron_variant | LOW | c.1230+7C>T| |
S184 |
6155 | BAA01g05110 | A01 | 2245810 | G | A | upstream_gene_variant | MODIFIER | c.-338G>A| |
S95 |
6156 | BAA01g05110 | A01 | 2246228 | C | T | synonymous_variant | LOW | c.81C>T|p.Pro27Pro |
S168 |
6157 | BAA01g05110 | A01 | 2246313 | G | A | splice_region_variant&intron_variant | LOW | c.109-8G>A| |
S272 |
6158 | BAA01g05110 | A01 | 2246320 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.109-1G>A| |
S123 |
6159 | BAA01g05110 | A01 | 2246457 | C | T | missense_variant | MODERATE | c.173C>T|p.Pro58Leu |
S249 |
6160 | BAA01g05110 | A01 | 2247388 | G | A | missense_variant | MODERATE | c.542G>A|p.Gly181Glu |
S191 |
6161 | BAA01g05110 | A01 | 2247447 | C | T | missense_variant | MODERATE | c.601C>T|p.Pro201Ser |
S68 |
6162 | BAA01g05120 | A01 | 2249431 | C | T | missense_variant | MODERATE | c.199C>T|p.Leu67Phe |
S264 |
6163 | BAA01g05120 | A01 | 2249445 | C | T | synonymous_variant | LOW | c.213C>T|p.Val71Val |
S244 |
6164 | BAA01g05120 | A01 | 2250479 | G | A | stop_gained | HIGH | c.1178G>A|p.Trp393* |
S37 |
6165 | BAA01g05120 | A01 | 2250955 | G | A | missense_variant | MODERATE | c.1444G>A|p.Asp482Asn |
S224 |
6166 | BAA01g05120 | A01 | 2251589 | C | T | missense_variant | MODERATE | c.1985C>T|p.Thr662Ile |
S140 |
6167 | BAA01g05120 | A01 | 2251939 | G | A | missense_variant | MODERATE | c.2335G>A|p.Asp779Asn |
S208 S219 |
6168 | BAA01g05120 | A01 | 2252040 | G | A | synonymous_variant | LOW | c.2436G>A|p.Thr812Thr |
S105 S106 |
6169 | BAA01g05120 | A01 | 2252941 | G | A | missense_variant | MODERATE | c.2896G>A|p.Ala966Thr |
S204 |
6170 | BAA01g05130 | A01 | 2253332 | G | A | downstream_gene_variant | MODIFIER | c.*2886C>T| |
S10 |
6171 | BAA01g05120 | A01 | 2253744 | G | A | missense_variant | MODERATE | c.3278G>A|p.Gly1093Glu |
S242 |
6172 | BAA01g05120 | A01 | 2253908 | C | T | missense_variant | MODERATE | c.3442C>T|p.Leu1148Phe |
S246 |
6173 | BAA01g05120 | A01 | 2254154 | C | T | missense_variant | MODERATE | c.3688C>T|p.Pro1230Ser |
S164 |
6174 | BAA01g05120 | A01 | 2254266 | C | T | missense_variant | MODERATE | c.3800C>T|p.Pro1267Leu |
S66 |
6175 | BAA01g05120 | A01 | 2254276 | C | T | synonymous_variant | LOW | c.3810C>T|p.Tyr1270Tyr |
S221 |