| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 45651 | BAA01g27270 | A01 | 15668637 | G | A | upstream_gene_variant | MODIFIER | c.-1124G>A| |
S140 |
| 45652 | BAA01g27270 | A01 | 15668640 | G | A | upstream_gene_variant | MODIFIER | c.-1121G>A| |
S63 |
| 45653 | BAA01g27270 | A01 | 15668749 | G | A | upstream_gene_variant | MODIFIER | c.-1012G>A| |
S12 |
| 45654 | BAA01g27270 | A01 | 15668836 | G | A | upstream_gene_variant | MODIFIER | c.-925G>A| |
S216 |
| 45655 | BAA01g27270 | A01 | 15669140 | C | T | upstream_gene_variant | MODIFIER | c.-621C>T| |
S239 |
| 45656 | BAA01g27270 | A01 | 15669369 | G | A | upstream_gene_variant | MODIFIER | c.-392G>A| |
S138 |
| 45657 | BAA01g27270 | A01 | 15669622 | C | T | upstream_gene_variant | MODIFIER | c.-139C>T| |
S11 |
| 45658 | BAA01g27270 | A01 | 15669694 | C | T | upstream_gene_variant | MODIFIER | c.-67C>T| |
S18 |
| 45659 | BAA01g27270 | A01 | 15670282 | G | A | synonymous_variant | LOW | c.219G>A|p.Glu73Glu |
S80 |
| 45660 | BAA01g27270 | A01 | 15670442 | A | T | missense_variant | MODERATE | c.379A>T|p.Ile127Leu |
S197 |
| 45661 | BAA01g27270 | A01 | 15670460 | C | T | missense_variant | MODERATE | c.397C>T|p.Leu133Phe |
S261 |
| 45662 | BAA01g27270 | A01 | 15670806 | C | T | downstream_gene_variant | MODIFIER | c.*335C>T| |
S284 |
| 45663 | BAA01g27270 | A01 | 15670942 | G | A | downstream_gene_variant | MODIFIER | c.*471G>A| |
S161 |
| 45664 | BAA01g27270 | A01 | 15670954 | C | T | downstream_gene_variant | MODIFIER | c.*483C>T| |
S206 S26 |
| 45665 | BAA01g27270 | A01 | 15671185 | G | A | downstream_gene_variant | MODIFIER | c.*714G>A| |
S251 |
| 45666 | BAA01g27270 | A01 | 15671706 | C | T | downstream_gene_variant | MODIFIER | c.*1235C>T| |
S146 |
| 45667 | BAA01g27280 | A01 | 15673307 | G | A | synonymous_variant | LOW | c.1215C>T|p.Ser405Ser |
S98 |
| 45668 | BAA01g27270 | A01 | 15673785 | C | T | downstream_gene_variant | MODIFIER | c.*3314C>T| |
S182 |
| 45669 | BAA01g27280 | A01 | 15674124 | G | A | synonymous_variant | LOW | c.972C>T|p.Phe324Phe |
S298 |
| 45670 | BAA01g27270 | A01 | 15674365 | C | T | downstream_gene_variant | MODIFIER | c.*3894C>T| |
S249 |
| 45671 | BAA01g27280 | A01 | 15674869 | C | T | missense_variant | MODERATE | c.550G>A|p.Glu184Lys |
S67 |
| 45672 | BAA01g27280 | A01 | 15675524 | C | T | intron_variant | MODIFIER | c.408+25G>A| |
S81 S85 |
| 45673 | BAA01g27280 | A01 | 15675760 | C | T | missense_variant&splice_region_variant | MODERATE | c.197G>A|p.Arg66Gln |
S61 |
| 45674 | BAA01g27280 | A01 | 15675963 | C | T | synonymous_variant | LOW | c.72G>A|p.Arg24Arg |
S208 S219 |
| 45675 | BAA01g27280 | A01 | 15676766 | G | A | upstream_gene_variant | MODIFIER | c.-732C>T| |
S201 |