Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30640 | A02 | 17966829 | G | A | upstream_gene_variant | MODIFIER | c.-4838G>A| |
S156 |
2 | BAA02g30640 | A02 | 17966978 | C | T | upstream_gene_variant | MODIFIER | c.-4689C>T| |
S264 |
3 | BAA02g30640 | A02 | 17967430 | G | A | upstream_gene_variant | MODIFIER | c.-4237G>A| |
S263 |
4 | BAA02g30640 | A02 | 17968306 | A | T | upstream_gene_variant | MODIFIER | c.-3361A>T| |
S189 |
5 | BAA02g30640 | A02 | 17969128 | C | T | upstream_gene_variant | MODIFIER | c.-2539C>T| |
S303 |
6 | BAA02g30640 | A02 | 17971082 | G | A | upstream_gene_variant | MODIFIER | c.-585G>A| |
S85 |
7 | BAA02g30640 | A02 | 17971511 | C | T | upstream_gene_variant | MODIFIER | c.-156C>T| |
S255 |
8 | BAA02g30640 | A02 | 17971629 | C | T | upstream_gene_variant | MODIFIER | c.-38C>T| |
S177 |
9 | BAA02g30640 | A02 | 17971835 | C | T | missense_variant | MODERATE | c.169C>T|p.Pro57Ser |
S9 |
10 | BAA02g30640 | A02 | 17971961 | C | T | intron_variant | MODIFIER | c.220+75C>T| |
S289 S290 |
11 | BAA02g30640 | A02 | 17972398 | C | T | intron_variant | MODIFIER | c.221-64C>T| |
S87 |
12 | BAA02g30640 | A02 | 17972601 | G | A | missense_variant | MODERATE | c.286G>A|p.Asp96Asn |
S136 |
13 | BAA02g30640 | A02 | 17972721 | C | T | intron_variant | MODIFIER | c.335-15C>T| |
S171 |
14 | BAA02g30640 | A02 | 17973022 | G | A | missense_variant | MODERATE | c.555G>A|p.Met185Ile |
S148 S210 S30 S31 |
15 | BAA02g30640 | A02 | 17974825 | G | A | downstream_gene_variant | MODIFIER | c.*1362G>A| |
S265 |
16 | BAA02g30640 | A02 | 17975308 | G | A | downstream_gene_variant | MODIFIER | c.*1845G>A| |
S153 S213 |
17 | BAA02g30640 | A02 | 17975368 | C | T | downstream_gene_variant | MODIFIER | c.*1905C>T| |
S273 |
18 | BAA02g30640 | A02 | 17975439 | G | A | downstream_gene_variant | MODIFIER | c.*1976G>A| |
S162 |
19 | BAA02g30640 | A02 | 17975578 | G | A | downstream_gene_variant | MODIFIER | c.*2115G>A| |
S166 |
20 | BAA02g30640 | A02 | 17975580 | G | A | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S25 |
21 | BAA02g30640 | A02 | 17977262 | G | A | downstream_gene_variant | MODIFIER | c.*3799G>A| |
S13 |
22 | BAA02g30640 | A02 | 17977347 | G | A | downstream_gene_variant | MODIFIER | c.*3884G>A| |
S205 |
23 | BAA02g30640 | A02 | 17977652 | C | T | downstream_gene_variant | MODIFIER | c.*4189C>T| |
S180 |
24 | BAA02g30640 | A02 | 17977660 | C | T | downstream_gene_variant | MODIFIER | c.*4197C>T| |
S136 |
25 | BAA02g30640 | A02 | 17977816 | C | T | downstream_gene_variant | MODIFIER | c.*4353C>T| |
S6 |