Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g10100 | A07 | 18996463 | C | T | upstream_gene_variant | MODIFIER | c.-2965C>T| |
S42 |
2 | BAA07g10100 | A07 | 18996497 | C | T | upstream_gene_variant | MODIFIER | c.-2931C>T| |
S259 |
3 | BAA07g10100 | A07 | 18996851 | C | T | upstream_gene_variant | MODIFIER | c.-2577C>T| |
S216 |
4 | BAA07g10100 | A07 | 18996960 | C | T | upstream_gene_variant | MODIFIER | c.-2468C>T| |
S70 |
5 | BAA07g10100 | A07 | 18997606 | C | T | upstream_gene_variant | MODIFIER | c.-1822C>T| |
S256 |
6 | BAA07g10100 | A07 | 18998226 | G | A | upstream_gene_variant | MODIFIER | c.-1202G>A| |
S111 |
7 | BAA07g10100 | A07 | 18998423 | C | T | upstream_gene_variant | MODIFIER | c.-1005C>T| |
S179 |
8 | BAA07g10100 | A07 | 18998640 | G | A | upstream_gene_variant | MODIFIER | c.-788G>A| |
S87 |
9 | BAA07g10100 | A07 | 18998906 | C | T | upstream_gene_variant | MODIFIER | c.-522C>T| |
S42 |
10 | BAA07g10100 | A07 | 18998962 | C | T | upstream_gene_variant | MODIFIER | c.-466C>T| |
S296 |
11 | BAA07g10100 | A07 | 18999325 | C | T | upstream_gene_variant | MODIFIER | c.-103C>T| |
S256 |
12 | BAA07g10100 | A07 | 18999370 | G | A | upstream_gene_variant | MODIFIER | c.-58G>A| |
S223 |
13 | BAA07g10100 | A07 | 18999478 | C | T | synonymous_variant | LOW | c.51C>T|p.Ala17Ala |
S104 |
14 | BAA07g10100 | A07 | 18999629 | G | A | missense_variant | MODERATE | c.202G>A|p.Glu68Lys |
S237 |
15 | BAA07g10100 | A07 | 18999681 | C | T | missense_variant | MODERATE | c.254C>T|p.Thr85Ile |
S42 |
16 | BAA07g10100 | A07 | 19000057 | G | A | missense_variant | MODERATE | c.535G>A|p.Glu179Lys |
S308 |
17 | BAA07g10100 | A07 | 19001064 | C | T | missense_variant | MODERATE | c.1000C>T|p.His334Tyr |
S148 S210 S30 S31 |
18 | BAA07g10100 | A07 | 19002735 | G | A | missense_variant | MODERATE | c.2069G>A|p.Gly690Glu |
S87 |
19 | BAA07g10100 | A07 | 19002824 | G | A | missense_variant | MODERATE | c.2158G>A|p.Ala720Thr |
S288 |
20 | BAA07g10100 | A07 | 19006107 | G | C | downstream_gene_variant | MODIFIER | c.*2891G>C| |
S204 |
21 | BAA07g10100 | A07 | 19007677 | G | A | downstream_gene_variant | MODIFIER | c.*4461G>A| |
S108 |