Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2601 | BAA01g02120 | A01 | 968823 | C | T | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S249 |
2602 | BAA01g02110 | A01 | 969211 | C | T | missense_variant | MODERATE | c.1303G>A|p.Glu435Lys |
S8 |
2603 | BAA01g02110 | A01 | 969292 | C | T | missense_variant | MODERATE | c.1222G>A|p.Asp408Asn |
S255 |
2604 | BAA01g02110 | A01 | 969327 | C | T | missense_variant | MODERATE | c.1187G>A|p.Cys396Tyr |
S189 |
2605 | BAA01g02110 | A01 | 969546 | C | T | missense_variant | MODERATE | c.968G>A|p.Gly323Glu |
S75 S81 |
2606 | BAA01g02110 | A01 | 969695 | C | T | synonymous_variant | LOW | c.819G>A|p.Lys273Lys |
S117 |
2607 | BAA01g02110 | A01 | 971343 | C | T | upstream_gene_variant | MODIFIER | c.-542G>A| |
S25 |
2608 | BAA01g02120 | A01 | 971681 | G | A | synonymous_variant | LOW | c.165G>A|p.Glu55Glu |
S10 |
2609 | BAA01g02120 | A01 | 971780 | G | A | synonymous_variant | LOW | c.264G>A|p.Glu88Glu |
S229 |
2610 | BAA01g02120 | A01 | 971882 | C | T | synonymous_variant | LOW | c.366C>T|p.Ala122Ala |
S267 |
2611 | BAA01g02110 | A01 | 973005 | G | A | upstream_gene_variant | MODIFIER | c.-2204C>T| |
S15 S3 |
2612 | BAA01g02110 | A01 | 973460 | G | A | upstream_gene_variant | MODIFIER | c.-2659C>T| |
S293 |
2613 | BAA01g02110 | A01 | 974425 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S113 |
2614 | BAA01g02130 | A01 | 974598 | G | A | missense_variant | MODERATE | c.129G>A|p.Met43Ile |
S133 |
2615 | BAA01g02130 | A01 | 975442 | G | A | missense_variant | MODERATE | c.538G>A|p.Ala180Thr |
S293 |
2616 | BAA01g02120 | A01 | 976271 | G | A | downstream_gene_variant | MODIFIER | c.*4227G>A| |
S306 S308 |
2617 | BAA01g02130 | A01 | 976527 | G | A | missense_variant | MODERATE | c.1126G>A|p.Asp376Asn |
S276 |
2618 | BAA01g02120 | A01 | 976738 | C | T | downstream_gene_variant | MODIFIER | c.*4694C>T| |
S160 |
2619 | BAA01g02140 | A01 | 977173 | G | A | missense_variant | MODERATE | c.1910C>T|p.Pro637Leu |
S162 |
2620 | BAA01g02140 | A01 | 977426 | G | A | missense_variant | MODERATE | c.1657C>T|p.Pro553Ser |
S124 |
2621 | BAA01g02130 | A01 | 980201 | C | T | downstream_gene_variant | MODIFIER | c.*3350C>T| |
S179 |
2622 | BAA01g02140 | A01 | 981214 | C | T | missense_variant | MODERATE | c.278G>A|p.Arg93Lys |
S236 |
2623 | BAA01g02140 | A01 | 981768 | G | A | upstream_gene_variant | MODIFIER | c.-277C>T| |
S67 |
2624 | BAA01g02140 | A01 | 982672 | C | T | upstream_gene_variant | MODIFIER | c.-1181G>A| |
S155 S211 |
2625 | BAA01g02140 | A01 | 982741 | C | T | upstream_gene_variant | MODIFIER | c.-1250G>A| |
S135 |