Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18480 | A05 | 10614788 | G | A | upstream_gene_variant | MODIFIER | c.-3594G>A| |
S15 |
2 | BAA05g18480 | A05 | 10615579 | C | T | upstream_gene_variant | MODIFIER | c.-2803C>T| |
S211 S227 |
3 | BAA05g18480 | A05 | 10617985 | G | A | upstream_gene_variant | MODIFIER | c.-397G>A| |
S11 |
4 | BAA05g18480 | A05 | 10618007 | C | T | upstream_gene_variant | MODIFIER | c.-375C>T| |
S267 |
5 | BAA05g18480 | A05 | 10618012 | C | T | upstream_gene_variant | MODIFIER | c.-370C>T| |
S121 |
6 | BAA05g18480 | A05 | 10618153 | C | T | upstream_gene_variant | MODIFIER | c.-229C>T| |
S84 S93 |
7 | BAA05g18480 | A05 | 10618352 | G | A | upstream_gene_variant | MODIFIER | c.-30G>A| |
S122 |
8 | BAA05g18480 | A05 | 10620236 | G | A | synonymous_variant | LOW | c.1035G>A|p.Lys345Lys |
S25 |
9 | BAA05g18480 | A05 | 10622398 | G | A | missense_variant | MODERATE | c.1249G>A|p.Asp417Asn |
S179 |
10 | BAA05g18480 | A05 | 10622431 | G | A | missense_variant | MODERATE | c.1282G>A|p.Glu428Lys |
S80 |
11 | BAA05g18480 | A05 | 10622465 | C | T | missense_variant | MODERATE | c.1316C>T|p.Thr439Ile |
S45 |
12 | BAA05g18480 | A05 | 10625402 | C | T | downstream_gene_variant | MODIFIER | c.*2828C>T| |
S242 |
13 | BAA05g18480 | A05 | 10626361 | G | A | downstream_gene_variant | MODIFIER | c.*3787G>A| |
S118 S23 |
14 | BAA05g18480 | A05 | 10626430 | C | T | downstream_gene_variant | MODIFIER | c.*3856C>T| |
S305 |