Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17070 | A06 | 8579819 | C | T | upstream_gene_variant | MODIFIER | c.-4078C>T| |
S112 |
2 | BAA06g17070 | A06 | 8580080 | G | A | upstream_gene_variant | MODIFIER | c.-3817G>A| |
S204 |
3 | BAA06g17070 | A06 | 8580676 | G | A | upstream_gene_variant | MODIFIER | c.-3221G>A| |
S264 |
4 | BAA06g17070 | A06 | 8581376 | C | T | upstream_gene_variant | MODIFIER | c.-2521C>T| |
S205 |
5 | BAA06g17070 | A06 | 8581655 | G | A | upstream_gene_variant | MODIFIER | c.-2242G>A| |
S280 |
6 | BAA06g17070 | A06 | 8582075 | C | T | upstream_gene_variant | MODIFIER | c.-1822C>T| |
S95 |
7 | BAA06g17070 | A06 | 8582084 | C | T | upstream_gene_variant | MODIFIER | c.-1813C>T| |
S25 |
8 | BAA06g17070 | A06 | 8582713 | C | T | upstream_gene_variant | MODIFIER | c.-1184C>T| |
S200 |
9 | BAA06g17070 | A06 | 8582959 | C | T | upstream_gene_variant | MODIFIER | c.-938C>T| |
S109 |
10 | BAA06g17070 | A06 | 8583932 | G | A | synonymous_variant | LOW | c.36G>A|p.Gln12Gln |
S270 |
11 | BAA06g17070 | A06 | 8584748 | C | T | missense_variant | MODERATE | c.374C>T|p.Thr125Ile |
S263 |
12 | BAA06g17070 | A06 | 8586138 | C | T | missense_variant | MODERATE | c.1450C>T|p.Leu484Phe |
S293 |