Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04660 | A09 | 2711318 | G | A | upstream_gene_variant | MODIFIER | c.-3363G>A| |
S15 S3 |
2 | BAA09g04660 | A09 | 2711490 | G | A | upstream_gene_variant | MODIFIER | c.-3191G>A| |
S4 |
3 | BAA09g04660 | A09 | 2711624 | C | T | upstream_gene_variant | MODIFIER | c.-3057C>T| |
S169 |
4 | BAA09g04660 | A09 | 2712074 | G | A | upstream_gene_variant | MODIFIER | c.-2607G>A| |
S302 |
5 | BAA09g04660 | A09 | 2713033 | G | A | upstream_gene_variant | MODIFIER | c.-1648G>A| |
S190 |
6 | BAA09g04660 | A09 | 2715697 | C | T | synonymous_variant | LOW | c.1017C>T|p.Leu339Leu |
S179 |
7 | BAA09g04660 | A09 | 2715876 | G | A | missense_variant | MODERATE | c.1196G>A|p.Gly399Glu |
S108 |
8 | BAA09g04660 | A09 | 2715890 | G | A | missense_variant | MODERATE | c.1210G>A|p.Glu404Lys |
S274 |
9 | BAA09g04660 | A09 | 2716788 | C | T | missense_variant | MODERATE | c.2108C>T|p.Thr703Ile |
S173 |
10 | BAA09g04660 | A09 | 2716889 | G | A | missense_variant | MODERATE | c.2209G>A|p.Val737Ile |
S114 |
11 | BAA09g04660 | A09 | 2717459 | G | A | missense_variant | MODERATE | c.2779G>A|p.Asp927Asn |
S45 |
12 | BAA09g04660 | A09 | 2718056 | C | T | missense_variant | MODERATE | c.2942C>T|p.Thr981Ile |
S284 |