Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09220 | A05 | 4612234 | G | A | upstream_gene_variant | MODIFIER | c.-4152G>A| |
S294 |
2 | BAA05g09220 | A05 | 4612701 | G | A | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S41 |
3 | BAA05g09220 | A05 | 4613181 | C | T | upstream_gene_variant | MODIFIER | c.-3205C>T| |
S18 |
4 | BAA05g09220 | A05 | 4613487 | G | A | upstream_gene_variant | MODIFIER | c.-2899G>A| |
S157 |
5 | BAA05g09220 | A05 | 4614073 | C | A | upstream_gene_variant | MODIFIER | c.-2313C>A| |
S297 |
6 | BAA05g09220 | A05 | 4615110 | G | A | upstream_gene_variant | MODIFIER | c.-1276G>A| |
S173 |
7 | BAA05g09220 | A05 | 4618018 | G | A | synonymous_variant | LOW | c.1395G>A|p.Glu465Glu |
S112 |
8 | BAA05g09220 | A05 | 4618431 | G | A | missense_variant | MODERATE | c.1657G>A|p.Ala553Thr |
S165 |
9 | BAA05g09220 | A05 | 4619088 | G | A | missense_variant | MODERATE | c.2314G>A|p.Gly772Arg |
S244 |
10 | BAA05g09220 | A05 | 4620053 | G | A | splice_donor_variant&intron_variant | HIGH | c.3023+1G>A| |
S246 |
11 | BAA05g09220 | A05 | 4620614 | G | A | synonymous_variant | LOW | c.3216G>A|p.Ala1072Ala |
S178 |
12 | BAA05g09220 | A05 | 4620636 | G | A | missense_variant | MODERATE | c.3238G>A|p.Glu1080Lys |
S94 |
13 | BAA05g09220 | A05 | 4620671 | G | A | synonymous_variant | LOW | c.3273G>A|p.Gln1091Gln |
S95 |
14 | BAA05g09220 | A05 | 4620811 | C | T | missense_variant | MODERATE | c.3413C>T|p.Ala1138Val |
S270 |
15 | BAA05g09220 | A05 | 4620881 | C | T | synonymous_variant | LOW | c.3483C>T|p.Phe1161Phe |
S247 |
16 | BAA05g09220 | A05 | 4626947 | C | T | downstream_gene_variant | MODIFIER | c.*4672C>T| |
S203 |