Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g23460 | A05 | 28110399 | C | T | upstream_gene_variant | MODIFIER | c.-4606C>T| |
S94 |
2 | BAA05g23460 | A05 | 28110917 | G | A | upstream_gene_variant | MODIFIER | c.-4088G>A| |
S247 |
3 | BAA05g23460 | A05 | 28110919 | G | A | upstream_gene_variant | MODIFIER | c.-4086G>A| |
S62 |
4 | BAA05g23460 | A05 | 28113609 | G | A | upstream_gene_variant | MODIFIER | c.-1396G>A| |
S129 |
5 | BAA05g23460 | A05 | 28114457 | G | A | upstream_gene_variant | MODIFIER | c.-548G>A| |
S270 |
6 | BAA05g23460 | A05 | 28114879 | C | T | upstream_gene_variant | MODIFIER | c.-126C>T| |
S242 |
7 | BAA05g23460 | A05 | 28115076 | G | A | synonymous_variant | LOW | c.72G>A|p.Glu24Glu |
S302 |
8 | BAA05g23460 | A05 | 28115155 | G | A | missense_variant | MODERATE | c.151G>A|p.Asp51Asn |
S109 |
9 | BAA05g23460 | A05 | 28115681 | C | T | synonymous_variant | LOW | c.528C>T|p.Phe176Phe |
S229 |
10 | BAA05g23460 | A05 | 28115720 | G | A | intron_variant | MODIFIER | c.537+30G>A| |
S152 |
11 | BAA05g23460 | A05 | 28117453 | G | A | missense_variant | MODERATE | c.1574G>A|p.Gly525Asp |
S112 |
12 | BAA05g23460 | A05 | 28117825 | C | T | synonymous_variant | LOW | c.1779C>T|p.Ala593Ala |
S47 |
13 | BAA05g23460 | A05 | 28118212 | G | A | downstream_gene_variant | MODIFIER | c.*318G>A| |
S173 |
14 | BAA05g23460 | A05 | 28119673 | G | A | downstream_gene_variant | MODIFIER | c.*1779G>A| |
S190 |
15 | BAA05g23460 | A05 | 28119978 | G | T | downstream_gene_variant | MODIFIER | c.*2084G>T| |
S84 S93 |
16 | BAA05g23460 | A05 | 28120085 | G | A | downstream_gene_variant | MODIFIER | c.*2191G>A| |
S180 S306 |
17 | BAA05g23460 | A05 | 28121607 | C | T | downstream_gene_variant | MODIFIER | c.*3713C>T| |
S261 |
18 | BAA05g23460 | A05 | 28122035 | C | T | downstream_gene_variant | MODIFIER | c.*4141C>T| |
S204 |