| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 30851 | BAA01g21500 | A01 | 10667337 | G | A | upstream_gene_variant | MODIFIER | c.-1861G>A| |
S199 |
| 30852 | BAA01g21500 | A01 | 10668524 | C | T | upstream_gene_variant | MODIFIER | c.-674C>T| |
S200 S3 |
| 30853 | BAA01g21500 | A01 | 10668641 | G | A | upstream_gene_variant | MODIFIER | c.-557G>A| |
S204 |
| 30854 | BAA01g21500 | A01 | 10668649 | C | T | upstream_gene_variant | MODIFIER | c.-549C>T| |
S44 |
| 30855 | BAA01g21500 | A01 | 10669127 | G | A | upstream_gene_variant | MODIFIER | c.-71G>A| |
S209 |
| 30856 | BAA01g21500 | A01 | 10669201 | G | A | missense_variant | MODERATE | c.4G>A|p.Ala2Thr |
S9 |
| 30857 | BAA01g21500 | A01 | 10669526 | C | T | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S10 |
| 30858 | BAA01g21500 | A01 | 10669871 | C | T | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S255 |
| 30859 | BAA01g21500 | A01 | 10669921 | G | A | missense_variant | MODERATE | c.529G>A|p.Gly177Ser |
S57 |
| 30860 | BAA01g21510 | A01 | 10670132 | G | A | upstream_gene_variant | MODIFIER | c.-1001G>A| |
S199 |
| 30861 | BAA01g21510 | A01 | 10670717 | G | A | upstream_gene_variant | MODIFIER | c.-416G>A| |
S110 |
| 30862 | BAA01g21500 | A01 | 10671186 | C | T | downstream_gene_variant | MODIFIER | c.*1116C>T| |
S143 |
| 30863 | BAA01g21500 | A01 | 10671191 | C | T | downstream_gene_variant | MODIFIER | c.*1121C>T| |
S42 |
| 30864 | BAA01g21510 | A01 | 10671450 | G | A | missense_variant | MODERATE | c.205G>A|p.Val69Ile |
S80 |
| 30865 | BAA01g21510 | A01 | 10671622 | C | T | missense_variant | MODERATE | c.377C>T|p.Pro126Leu |
S238 |
| 30866 | BAA01g21510 | A01 | 10671631 | C | T | missense_variant&splice_region_variant | MODERATE | c.386C>T|p.Thr129Ile |
S148 S210 |
| 30867 | BAA01g21510 | A01 | 10672262 | C | T | missense_variant | MODERATE | c.716C>T|p.Ser239Phe |
S117 |
| 30868 | BAA01g21500 | A01 | 10672847 | C | T | downstream_gene_variant | MODIFIER | c.*2777C>T| |
S146 |
| 30869 | BAA01g21500 | A01 | 10673094 | G | A | downstream_gene_variant | MODIFIER | c.*3024G>A| |
S13 |
| 30870 | BAA01g21500 | A01 | 10673444 | G | A | downstream_gene_variant | MODIFIER | c.*3374G>A| |
S144 |
| 30871 | BAA01g21520 | A01 | 10673800 | C | T | missense_variant | MODERATE | c.353G>A|p.Cys118Tyr |
S17 |
| 30872 | BAA01g21520 | A01 | 10673805 | G | A | synonymous_variant | LOW | c.348C>T|p.Cys116Cys |
S163 |
| 30873 | BAA01g21520 | A01 | 10674068 | C | T | missense_variant | MODERATE | c.85G>A|p.Glu29Lys |
S230 |
| 30874 | BAA01g21520 | A01 | 10674079 | C | T | missense_variant | MODERATE | c.74G>A|p.Arg25Gln |
S128 |
| 30875 | BAA01g21520 | A01 | 10674501 | G | A | upstream_gene_variant | MODIFIER | c.-349C>T| |
S45 |