Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7451 | BAA01g06030 | A01 | 2706890 | C | T | upstream_gene_variant | MODIFIER | c.-48G>A| |
S158 |
7452 | BAA01g06030 | A01 | 2707743 | C | T | upstream_gene_variant | MODIFIER | c.-901G>A| |
S104 S52 |
7453 | BAA01g06030 | A01 | 2707948 | C | T | upstream_gene_variant | MODIFIER | c.-1106G>A| |
S296 |
7454 | BAA01g06030 | A01 | 2708107 | C | T | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S63 |
7455 | BAA01g06040 | A01 | 2709326 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.391-1G>A| |
S35 |
7456 | BAA01g06030 | A01 | 2710978 | C | T | upstream_gene_variant | MODIFIER | c.-4136G>A| |
S203 |
7457 | BAA01g06030 | A01 | 2711187 | G | A | upstream_gene_variant | MODIFIER | c.-4345C>T| |
S86 |
7458 | BAA01g06050 | A01 | 2713686 | G | A | missense_variant | MODERATE | c.1375C>T|p.Leu459Phe |
S209 |
7459 | BAA01g06050 | A01 | 2713723 | G | A | synonymous_variant | LOW | c.1338C>T|p.Ile446Ile |
S57 |
7460 | BAA01g06050 | A01 | 2714050 | C | T | synonymous_variant | LOW | c.1011G>A|p.Glu337Glu |
S270 |
7461 | BAA01g06040 | A01 | 2715101 | C | T | upstream_gene_variant | MODIFIER | c.-4967G>A| |
S103 |
7462 | BAA01g06050 | A01 | 2715211 | C | T | upstream_gene_variant | MODIFIER | c.-151G>A| |
S164 |
7463 | BAA01g06050 | A01 | 2716547 | G | A | upstream_gene_variant | MODIFIER | c.-1487C>T| |
S299 |
7464 | BAA01g06060 | A01 | 2717219 | G | A | missense_variant | MODERATE | c.475G>A|p.Glu159Lys |
S251 |
7465 | BAA01g06050 | A01 | 2718094 | C | T | upstream_gene_variant | MODIFIER | c.-3034G>A| |
S88 |
7466 | BAA01g06060 | A01 | 2718300 | G | A | synonymous_variant | LOW | c.1005G>A|p.Lys335Lys |
S32 |
7467 | BAA01g06060 | A01 | 2718309 | G | A | synonymous_variant | LOW | c.1014G>A|p.Pro338Pro |
S83 |
7468 | BAA01g06060 | A01 | 2718645 | G | A | missense_variant | MODERATE | c.1256G>A|p.Ser419Asn |
S96 |
7469 | BAA01g06060 | A01 | 2718807 | C | T | missense_variant | MODERATE | c.1418C>T|p.Ser473Phe |
S263 |
7470 | BAA01g06060 | A01 | 2719547 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1953-1G>A| |
S274 |
7471 | BAA01g06060 | A01 | 2721265 | G | A | downstream_gene_variant | MODIFIER | c.*1372G>A| |
S288 |
7472 | BAA01g06060 | A01 | 2721325 | G | A | downstream_gene_variant | MODIFIER | c.*1432G>A| |
S167 |
7473 | BAA01g06070 | A01 | 2721523 | G | A | missense_variant | MODERATE | c.148G>A|p.Glu50Lys |
S281 |
7474 | BAA01g06070 | A01 | 2721738 | C | T | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S38 |
7475 | BAA01g06070 | A01 | 2721853 | C | T | missense_variant | MODERATE | c.398C>T|p.Ser133Phe |
S129 |