Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08160 | A04 | 5564489 | C | T | upstream_gene_variant | MODIFIER | c.-2807C>T| |
S242 |
2 | BAA04g08160 | A04 | 5564594 | A | C | upstream_gene_variant | MODIFIER | c.-2702A>C| |
S124 S129 S161 S219 S304 S305 S37 S39 S50 S76 S97 |
3 | BAA04g08160 | A04 | 5567360 | G | A | missense_variant | MODERATE | c.65G>A|p.Gly22Glu |
S104 S52 |
4 | BAA04g08160 | A04 | 5567458 | G | A | missense_variant | MODERATE | c.163G>A|p.Val55Ile |
S87 |
5 | BAA04g08160 | A04 | 5567657 | G | A | synonymous_variant | LOW | c.282G>A|p.Arg94Arg |
S244 |
6 | BAA04g08160 | A04 | 5567869 | C | T | missense_variant | MODERATE | c.494C>T|p.Ala165Val |
S165 |
7 | BAA04g08160 | A04 | 5568460 | C | T | missense_variant | MODERATE | c.1085C>T|p.Ser362Phe |
S97 |
8 | BAA04g08160 | A04 | 5570178 | G | A | downstream_gene_variant | MODIFIER | c.*1369G>A| |
S241 |
9 | BAA04g08160 | A04 | 5570419 | C | T | downstream_gene_variant | MODIFIER | c.*1610C>T| |
S95 |
10 | BAA04g08160 | A04 | 5570442 | C | T | downstream_gene_variant | MODIFIER | c.*1633C>T| |
S165 |
11 | BAA04g08160 | A04 | 5571676 | G | A | downstream_gene_variant | MODIFIER | c.*2867G>A| |
S138 |
12 | BAA04g08160 | A04 | 5571843 | C | T | downstream_gene_variant | MODIFIER | c.*3034C>T| |
S32 |
13 | BAA04g08160 | A04 | 5573132 | G | A | downstream_gene_variant | MODIFIER | c.*4323G>A| |
S277 |
14 | BAA04g08160 | A04 | 5573287 | C | T | downstream_gene_variant | MODIFIER | c.*4478C>T| |
S294 |
15 | BAA04g08160 | A04 | 5573600 | G | A | downstream_gene_variant | MODIFIER | c.*4791G>A| |
S34 |