| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 136301 | BAA10g21950 | A10 | 19116603 | C | T | stop_gained | HIGH | c.1648C>T|p.Gln550* |
S48 |
| 136302 | BAA10g21950 | A10 | 19117365 | C | T | missense_variant | MODERATE | c.2240C>T|p.Ser747Phe |
S10 |
| 136303 | BAA10g21950 | A10 | 19117377 | G | A | missense_variant | MODERATE | c.2252G>A|p.Ser751Asn |
S295 |
| 136304 | BAA10g21950 | A10 | 19117920 | G | A | missense_variant | MODERATE | c.2795G>A|p.Arg932Lys |
S294 |
| 136305 | BAA10g21950 | A10 | 19117999 | C | T | synonymous_variant | LOW | c.2874C>T|p.Leu958Leu |
S133 |
| 136306 | BAA10g21950 | A10 | 19118539 | C | T | synonymous_variant | LOW | c.3414C>T|p.Ala1138Ala |
S283 |
| 136307 | BAA10g21950 | A10 | 19118997 | G | A | missense_variant | MODERATE | c.3872G>A|p.Cys1291Tyr |
S1 S90 |
| 136308 | BAA10g21950 | A10 | 19119176 | G | A | missense_variant | MODERATE | c.4051G>A|p.Val1351Ile |
S178 |
| 136309 | BAA10g21960 | A10 | 19119861 | G | A | upstream_gene_variant | MODIFIER | c.-1287G>A| |
S280 |
| 136310 | BAA10g21970 | A10 | 19121609 | G | A | upstream_gene_variant | MODIFIER | c.-428G>A| |
S180 |
| 136311 | BAA10g21970 | A10 | 19122115 | C | T | missense_variant | MODERATE | c.79C>T|p.Leu27Phe |
S266 |
| 136312 | BAA10g21970 | A10 | 19122575 | C | T | splice_region_variant&intron_variant | LOW | c.465-4C>T| |
S44 |
| 136313 | BAA10g21970 | A10 | 19122922 | C | T | missense_variant | MODERATE | c.808C>T|p.Arg270Trp |
S162 |
| 136314 | BAA10g21980 | A10 | 19123680 | C | T | missense_variant | MODERATE | c.665C>T|p.Ala222Val |
S115 |
| 136315 | BAA10g21980 | A10 | 19123691 | G | A | missense_variant | MODERATE | c.676G>A|p.Val226Ile |
S36 |
| 136316 | BAA10g21980 | A10 | 19124026 | G | A | missense_variant | MODERATE | c.917G>A|p.Gly306Glu |
S130 |
| 136317 | BAA10g21980 | A10 | 19124486 | C | T | synonymous_variant | LOW | c.1278C>T|p.Leu426Leu |
S189 |
| 136318 | BAA10g21980 | A10 | 19124571 | C | T | missense_variant | MODERATE | c.1363C>T|p.Leu455Phe |
S133 |
| 136319 | BAA10g21990 | A10 | 19125820 | G | A | missense_variant | MODERATE | c.707G>A|p.Gly236Glu |
S55 |
| 136320 | BAA10g22020 | A10 | 19126767 | G | A | upstream_gene_variant | MODIFIER | c.-1408G>A| |
S55 |
| 136321 | BAA10g22020 | A10 | 19129431 | C | T | synonymous_variant | LOW | c.1005C>T|p.Pro335Pro |
S70 |
| 136322 | BAA10g22020 | A10 | 19129764 | G | A | synonymous_variant | LOW | c.1338G>A|p.Lys446Lys |
S127 |
| 136323 | BAA10g22020 | A10 | 19129784 | C | T | missense_variant | MODERATE | c.1358C>T|p.Ala453Val |
S42 |
| 136324 | BAA10g22010 | A10 | 19131185 | G | A | upstream_gene_variant | MODIFIER | c.-4140C>T| |
S273 |
| 136325 | BAA10g22010 | A10 | 19131219 | C | T | upstream_gene_variant | MODIFIER | c.-4174G>A| |
S146 S232 |