Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12610 | A05 | 6477390 | C | T | synonymous_variant | LOW | c.2586G>A|p.Gln862Gln |
S67 |
2 | BAA05g12610 | A05 | 6477932 | G | A | stop_gained | HIGH | c.2128C>T|p.Gln710* |
S200 |
3 | BAA05g12610 | A05 | 6478604 | G | A | missense_variant | MODERATE | c.1613C>T|p.Ala538Val |
S32 |
4 | BAA05g12610 | A05 | 6478702 | C | T | synonymous_variant | LOW | c.1515G>A|p.Glu505Glu |
S105 S106 |
5 | BAA05g12610 | A05 | 6479537 | G | A | missense_variant | MODERATE | c.998C>T|p.Thr333Ile |
S192 |
6 | BAA05g12610 | A05 | 6479708 | G | A | missense_variant | MODERATE | c.827C>T|p.Pro276Leu |
S231 |
7 | BAA05g12610 | A05 | 6480099 | G | A | intron_variant | MODIFIER | c.600+123C>T| |
S249 |
8 | BAA05g12610 | A05 | 6481676 | G | A | missense_variant | MODERATE | c.56C>T|p.Pro19Leu |
S60 |
9 | BAA05g12610 | A05 | 6481704 | C | T | missense_variant | MODERATE | c.28G>A|p.Gly10Arg |
S12 |
10 | BAA05g12610 | A05 | 6483058 | C | T | upstream_gene_variant | MODIFIER | c.-1327G>A| |
S280 |
11 | BAA05g12610 | A05 | 6483230 | C | T | upstream_gene_variant | MODIFIER | c.-1499G>A| |
S81 |
12 | BAA05g12610 | A05 | 6484042 | C | T | upstream_gene_variant | MODIFIER | c.-2311G>A| |
S162 |
13 | BAA05g12610 | A05 | 6484863 | C | T | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S18 |
14 | BAA05g12610 | A05 | 6484928 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S130 |
15 | BAA05g12610 | A05 | 6485136 | C | T | upstream_gene_variant | MODIFIER | c.-3405G>A| |
S167 |
16 | BAA05g12610 | A05 | 6485319 | G | A | upstream_gene_variant | MODIFIER | c.-3588C>T| |
S64 |
17 | BAA05g12610 | A05 | 6485452 | C | T | upstream_gene_variant | MODIFIER | c.-3721G>A| |
S61 |
18 | BAA05g12610 | A05 | 6486160 | G | A | upstream_gene_variant | MODIFIER | c.-4429C>T| |
S247 |
19 | BAA05g12610 | A05 | 6486639 | G | A | upstream_gene_variant | MODIFIER | c.-4908C>T| |
S133 |