Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2751 | BAA01g02210 | A01 | 1016402 | G | A | missense_variant | MODERATE | c.673G>A|p.Glu225Lys |
S103 |
2752 | BAA01g02210 | A01 | 1016405 | G | A | missense_variant | MODERATE | c.676G>A|p.Asp226Asn |
S113 |
2753 | BAA01g02200 | A01 | 1017656 | G | A | upstream_gene_variant | MODIFIER | c.-4947C>T| |
S232 |
2754 | BAA01g02220 | A01 | 1018032 | C | T | missense_variant | MODERATE | c.64C>T|p.Leu22Phe |
S76 |
2755 | BAA01g02220 | A01 | 1018506 | G | A | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S174 S27 |
2756 | BAA01g02220 | A01 | 1018544 | G | A | synonymous_variant | LOW | c.576G>A|p.Gln192Gln |
S170 |
2757 | BAA01g02220 | A01 | 1019012 | G | A | synonymous_variant | LOW | c.1044G>A|p.Glu348Glu |
S195 |
2758 | BAA01g02220 | A01 | 1019020 | C | T | missense_variant | MODERATE | c.1052C>T|p.Ala351Val |
S45 |
2759 | BAA01g02230 | A01 | 1019775 | C | T | upstream_gene_variant | MODIFIER | c.-666C>T| |
S77 S82 |
2760 | BAA01g02230 | A01 | 1020105 | C | T | upstream_gene_variant | MODIFIER | c.-336C>T| |
S121 |
2761 | BAA01g02230 | A01 | 1020387 | G | A | upstream_gene_variant | MODIFIER | c.-54G>A| |
S32 |
2762 | BAA01g02210 | A01 | 1021178 | C | T | downstream_gene_variant | MODIFIER | c.*4537C>T| |
S1 S90 |
2763 | BAA01g02230 | A01 | 1021487 | C | T | synonymous_variant | LOW | c.294C>T|p.Tyr98Tyr |
S20 |
2764 | BAA01g02240 | A01 | 1023527 | G | A | missense_variant | MODERATE | c.1004C>T|p.Ala335Val |
S108 |
2765 | BAA01g02240 | A01 | 1024574 | G | A | synonymous_variant | LOW | c.276C>T|p.Leu92Leu |
S156 |
2766 | BAA01g02240 | A01 | 1025880 | A | C | upstream_gene_variant | MODIFIER | c.-830T>G| |
S298 |
2767 | BAA01g02240 | A01 | 1026215 | C | T | upstream_gene_variant | MODIFIER | c.-1165G>A| |
S203 |
2768 | BAA01g02250 | A01 | 1026306 | C | T | synonymous_variant | LOW | c.546G>A|p.Gly182Gly |
S218 |
2769 | BAA01g02250 | A01 | 1026464 | C | T | missense_variant | MODERATE | c.388G>A|p.Ala130Thr |
S100 |
2770 | BAA01g02250 | A01 | 1026588 | C | T | synonymous_variant | LOW | c.264G>A|p.Lys88Lys |
S176 |
2771 | BAA01g02240 | A01 | 1028537 | C | T | upstream_gene_variant | MODIFIER | c.-3487G>A| |
S170 |
2772 | BAA01g02250-BAA01g02260 | A01 | 1033268 | C | T | intergenic_region | MODIFIER | n.1033268C>T| |
S25 |
2773 | BAA01g02250-BAA01g02260 | A01 | 1040054 | G | A | intergenic_region | MODIFIER | n.1040054G>A| |
S257 |
2774 | BAA01g02260 | A01 | 1041393 | G | A | upstream_gene_variant | MODIFIER | c.-3735G>A| |
S32 |
2775 | BAA01g02260 | A01 | 1042894 | C | T | upstream_gene_variant | MODIFIER | c.-2234C>T| |
S171 |