| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 140851 | BAA10g25970 | A10 | 20756045 | G | A | missense_variant | MODERATE | c.80C>T|p.Ser27Phe |
S136 |
| 140852 | BAA10g25970 | A10 | 20756250 | G | A | upstream_gene_variant | MODIFIER | c.-126C>T| |
S66 |
| 140853 | BAA10g25980 | A10 | 20757263 | C | T | synonymous_variant | LOW | c.1728G>A|p.Lys576Lys |
S125 |
| 140854 | BAA10g25980 | A10 | 20758465 | C | T | missense_variant | MODERATE | c.908G>A|p.Gly303Glu |
S161 |
| 140855 | BAA10g25980 | A10 | 20758836 | C | T | synonymous_variant | LOW | c.537G>A|p.Glu179Glu |
S107 |
| 140856 | BAA10g25980 | A10 | 20762032 | C | T | upstream_gene_variant | MODIFIER | c.-2359G>A| |
S23 |
| 140857 | BAA10g25980 | A10 | 20762400 | G | A | upstream_gene_variant | MODIFIER | c.-2727C>T| |
S81 |
| 140858 | BAA10g25980 | A10 | 20762578 | G | A | upstream_gene_variant | MODIFIER | c.-2905C>T| |
S205 |
| 140859 | BAA10g25980 | A10 | 20764604 | C | T | upstream_gene_variant | MODIFIER | c.-4931G>A| |
S68 |
| 140860 | BAA10g25990 | A10 | 20764942 | C | T | downstream_gene_variant | MODIFIER | c.*3316C>T| |
S259 |
| 140861 | BAA10g25990 | A10 | 20764985 | C | T | downstream_gene_variant | MODIFIER | c.*3359C>T| |
S42 |
| 140862 | BAA10g26000 | A10 | 20765925 | C | T | synonymous_variant | LOW | c.195G>A|p.Lys65Lys |
S196 |
| 140863 | BAA10g26000 | A10 | 20767620 | G | A | upstream_gene_variant | MODIFIER | c.-54C>T| |
S279 S303 |
| 140864 | BAA10g26000 | A10 | 20768394 | C | T | upstream_gene_variant | MODIFIER | c.-828G>A| |
S299 |
| 140865 | BAA10g26000 | A10 | 20768483 | C | T | upstream_gene_variant | MODIFIER | c.-917G>A| |
S84 S93 |
| 140866 | BAA10g26010 | A10 | 20768760 | G | A | missense_variant | MODERATE | c.1586C>T|p.Ser529Phe |
S95 |
| 140867 | BAA10g26010 | A10 | 20769157 | C | T | missense_variant | MODERATE | c.1189G>A|p.Asp397Asn |
S46 |
| 140868 | BAA10g26010 | A10 | 20770220 | G | A | synonymous_variant | LOW | c.1110C>T|p.Asp370Asp |
S288 |
| 140869 | BAA10g26010 | A10 | 20770508 | C | T | synonymous_variant | LOW | c.822G>A|p.Glu274Glu |
S169 |
| 140870 | BAA10g26010 | A10 | 20771611 | C | T | missense_variant | MODERATE | c.70G>A|p.Glu24Lys |
S201 |
| 140871 | BAA10g26000 | A10 | 20771902 | C | T | upstream_gene_variant | MODIFIER | c.-4336G>A| |
S157 S163 |
| 140872 | BAA10g26020 | A10 | 20774289 | G | A | missense_variant | MODERATE | c.881C>T|p.Thr294Met |
S239 |
| 140873 | BAA10g26020 | A10 | 20775432 | C | T | missense_variant | MODERATE | c.205G>A|p.Glu69Lys |
S177 |
| 140874 | BAA10g26010 | A10 | 20776003 | G | A | upstream_gene_variant | MODIFIER | c.-4323C>T| |
S138 |
| 140875 | BAA10g26020 | A10 | 20776723 | G | A | upstream_gene_variant | MODIFIER | c.-1087C>T| |
S50 |