Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06660 | A08 | 5440186 | G | A | upstream_gene_variant | MODIFIER | c.-4979G>A| |
S136 |
2 | BAA08g06660 | A08 | 5440712 | C | T | upstream_gene_variant | MODIFIER | c.-4453C>T| |
S226 |
3 | BAA08g06660 | A08 | 5440770 | G | A | upstream_gene_variant | MODIFIER | c.-4395G>A| |
S38 |
4 | BAA08g06660 | A08 | 5441257 | G | A | upstream_gene_variant | MODIFIER | c.-3908G>A| |
S81 S85 |
5 | BAA08g06660 | A08 | 5442519 | C | T | upstream_gene_variant | MODIFIER | c.-2646C>T| |
S126 |
6 | BAA08g06660 | A08 | 5444752 | G | A | upstream_gene_variant | MODIFIER | c.-413G>A| |
S238 |
7 | BAA08g06660 | A08 | 5445351 | G | A | missense_variant | MODERATE | c.187G>A|p.Gly63Arg |
S301 S304 |
8 | BAA08g06660 | A08 | 5445801 | G | A | missense_variant | MODERATE | c.446G>A|p.Gly149Asp |
S39 |
9 | BAA08g06660 | A08 | 5446291 | C | T | missense_variant | MODERATE | c.767C>T|p.Ser256Phe |
S149 S47 |
10 | BAA08g06660 | A08 | 5447956 | G | A | downstream_gene_variant | MODIFIER | c.*323G>A| |
S263 |
11 | BAA08g06660 | A08 | 5448542 | C | T | downstream_gene_variant | MODIFIER | c.*909C>T| |
S270 |
12 | BAA08g06660 | A08 | 5449079 | C | T | downstream_gene_variant | MODIFIER | c.*1446C>T| |
S223 |
13 | BAA08g06660 | A08 | 5449162 | C | T | downstream_gene_variant | MODIFIER | c.*1529C>T| |
S86 |
14 | BAA08g06660 | A08 | 5449207 | G | A | downstream_gene_variant | MODIFIER | c.*1574G>A| |
S110 |
15 | BAA08g06660 | A08 | 5450143 | C | T | downstream_gene_variant | MODIFIER | c.*2510C>T| |
S169 |
16 | BAA08g06660 | A08 | 5451014 | G | A | downstream_gene_variant | MODIFIER | c.*3381G>A| |
S297 |
17 | BAA08g06660 | A08 | 5451775 | G | A | downstream_gene_variant | MODIFIER | c.*4142G>A| |
S237 |
18 | BAA08g06660 | A08 | 5451973 | G | A | downstream_gene_variant | MODIFIER | c.*4340G>A| |
S139 |
19 | BAA08g06660 | A08 | 5452009 | G | A | downstream_gene_variant | MODIFIER | c.*4376G>A| |
S146 |