| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 131551 | BAA10g18780 | A10 | 17480622 | G | A | missense_variant | MODERATE | c.421G>A|p.Glu141Lys |
S131 |
| 131552 | BAA10g18790 | A10 | 17481954 | G | A | upstream_gene_variant | MODIFIER | c.-4671G>A| |
S65 |
| 131553 | BAA10g18790 | A10 | 17482664 | C | T | upstream_gene_variant | MODIFIER | c.-3961C>T| |
S202 |
| 131554 | BAA10g18790 | A10 | 17483204 | C | T | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S51 |
| 131555 | BAA10g18790 | A10 | 17483879 | G | A | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S240 |
| 131556 | BAA10g18790 | A10 | 17484326 | C | T | upstream_gene_variant | MODIFIER | c.-2299C>T| |
S301 S304 |
| 131557 | BAA10g18790 | A10 | 17485301 | G | C | upstream_gene_variant | MODIFIER | c.-1324G>C| |
S49 |
| 131558 | BAA10g18790 | A10 | 17485400 | G | A | upstream_gene_variant | MODIFIER | c.-1225G>A| |
S205 |
| 131559 | BAA10g18790 | A10 | 17485644 | G | A | upstream_gene_variant | MODIFIER | c.-981G>A| |
S192 |
| 131560 | BAA10g18790 | A10 | 17485885 | G | A | upstream_gene_variant | MODIFIER | c.-740G>A| |
S206 |
| 131561 | BAA10g18790 | A10 | 17487254 | G | A | synonymous_variant | LOW | c.630G>A|p.Gly210Gly |
S250 |
| 131562 | BAA10g18790 | A10 | 17487270 | G | A | missense_variant | MODERATE | c.646G>A|p.Glu216Lys |
S151 S263 |
| 131563 | BAA10g18790 | A10 | 17487662 | G | A | stop_gained | HIGH | c.1038G>A|p.Trp346* |
S295 |
| 131564 | BAA10g18800 | A10 | 17488967 | G | A | synonymous_variant | LOW | c.135G>A|p.Lys45Lys |
S62 |
| 131565 | BAA10g18800 | A10 | 17489094 | G | A | missense_variant | MODERATE | c.262G>A|p.Glu88Lys |
S74 |
| 131566 | BAA10g18810 | A10 | 17490022 | C | T | upstream_gene_variant | MODIFIER | c.-78G>A| |
S266 |
| 131567 | BAA10g18810 | A10 | 17490857 | C | T | upstream_gene_variant | MODIFIER | c.-913G>A| |
S12 |
| 131568 | BAA10g18810 | A10 | 17491408 | C | T | upstream_gene_variant | MODIFIER | c.-1464G>A| |
S256 |
| 131569 | BAA10g18810 | A10 | 17493693 | G | A | upstream_gene_variant | MODIFIER | c.-3749C>T| |
S289 S290 |
| 131570 | BAA10g18810 | A10 | 17493940 | G | A | upstream_gene_variant | MODIFIER | c.-3996C>T| |
S69 |
| 131571 | BAA10g18820 | A10 | 17494458 | G | A | missense_variant | MODERATE | c.761G>A|p.Gly254Glu |
S165 |
| 131572 | BAA10g18830 | A10 | 17495006 | C | T | upstream_gene_variant | MODIFIER | c.-1573C>T| |
S259 |
| 131573 | BAA10g18820 | A10 | 17495558 | G | A | missense_variant | MODERATE | c.1352G>A|p.Ser451Asn |
S3 |
| 131574 | BAA10g18830 | A10 | 17496106 | C | T | upstream_gene_variant | MODIFIER | c.-473C>T| |
S206 |
| 131575 | BAA10g18820 | A10 | 17496868 | G | A | downstream_gene_variant | MODIFIER | c.*1186G>A| |
S203 |