| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 117651 | BAA10g10670-BAA10g10680 | A10 | 12456688 | G | A | intergenic_region | MODIFIER | n.12456688G>A| |
S165 |
| 117652 | BAA10g10680 | A10 | 12458607 | G | A | upstream_gene_variant | MODIFIER | c.-4294G>A| |
S202 |
| 117653 | BAA10g10680 | A10 | 12459027 | C | T | upstream_gene_variant | MODIFIER | c.-3874C>T| |
S23 |
| 117654 | BAA10g10680 | A10 | 12459508 | G | A | upstream_gene_variant | MODIFIER | c.-3393G>A| |
S198 |
| 117655 | BAA10g10680 | A10 | 12459566 | G | A | upstream_gene_variant | MODIFIER | c.-3335G>A| |
S192 |
| 117656 | BAA10g10680 | A10 | 12459849 | G | A | upstream_gene_variant | MODIFIER | c.-3052G>A| |
S139 |
| 117657 | BAA10g10680 | A10 | 12459991 | C | T | upstream_gene_variant | MODIFIER | c.-2910C>T| |
S236 |
| 117658 | BAA10g10680 | A10 | 12460470 | C | T | upstream_gene_variant | MODIFIER | c.-2431C>T| |
S308 |
| 117659 | BAA10g10680 | A10 | 12460568 | G | A | upstream_gene_variant | MODIFIER | c.-2333G>A| |
S82 S92 |
| 117660 | BAA10g10680 | A10 | 12461484 | C | T | upstream_gene_variant | MODIFIER | c.-1417C>T| |
S193 |
| 117661 | BAA10g10680 | A10 | 12462126 | G | A | upstream_gene_variant | MODIFIER | c.-775G>A| |
S278 |
| 117662 | BAA10g10680 | A10 | 12462315 | C | T | upstream_gene_variant | MODIFIER | c.-586C>T| |
S76 |
| 117663 | BAA10g10680 | A10 | 12463892 | G | A | missense_variant | MODERATE | c.992G>A|p.Ser331Asn |
S265 |
| 117664 | BAA10g10690 | A10 | 12464925 | C | T | upstream_gene_variant | MODIFIER | c.-1880C>T| |
S176 |
| 117665 | BAA10g10690 | A10 | 12465737 | G | A | upstream_gene_variant | MODIFIER | c.-1068G>A| |
S129 |
| 117666 | BAA10g10690 | A10 | 12465894 | G | A | upstream_gene_variant | MODIFIER | c.-911G>A| |
S4 |
| 117667 | BAA10g10690 | A10 | 12466160 | G | A | upstream_gene_variant | MODIFIER | c.-645G>A| |
S296 |
| 117668 | BAA10g10690 | A10 | 12466411 | G | A | upstream_gene_variant | MODIFIER | c.-394G>A| |
S138 |
| 117669 | BAA10g10690 | A10 | 12466678 | C | T | upstream_gene_variant | MODIFIER | c.-127C>T| |
S274 |
| 117670 | BAA10g10690 | A10 | 12466837 | C | T | synonymous_variant | LOW | c.33C>T|p.Ser11Ser |
S17 |
| 117671 | BAA10g10690 | A10 | 12466985 | G | A | splice_region_variant&intron_variant | LOW | c.92-5G>A| |
S303 |
| 117672 | BAA10g10690 | A10 | 12467551 | G | A | synonymous_variant | LOW | c.468G>A|p.Lys156Lys |
S55 |
| 117673 | BAA10g10690 | A10 | 12467962 | G | A | synonymous_variant | LOW | c.879G>A|p.Arg293Arg |
S198 |
| 117674 | BAA10g10690 | A10 | 12468042 | C | T | missense_variant | MODERATE | c.959C>T|p.Thr320Ile |
S20 |
| 117675 | BAA10g10690 | A10 | 12468114 | G | A | missense_variant | MODERATE | c.1031G>A|p.Arg344His |
S64 |