Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02140 | A10 | 1007346 | C | T | intron_variant | MODIFIER | c.513-154G>A| |
S235 |
2 | BAA10g02140 | A10 | 1007568 | C | T | intron_variant | MODIFIER | c.513-376G>A| |
S170 |
3 | BAA10g02140 | A10 | 1008064 | C | T | intron_variant | MODIFIER | c.513-872G>A| |
S61 |
4 | BAA10g02140 | A10 | 1013135 | A | T | intron_variant | MODIFIER | c.512+2441T>A| |
S188 |
5 | BAA10g02140 | A10 | 1013592 | T | A | intron_variant | MODIFIER | c.512+1984A>T| |
S169 |
6 | BAA10g02140 | A10 | 1013722 | G | A | intron_variant | MODIFIER | c.512+1854C>T| |
S45 |
7 | BAA10g02140 | A10 | 1015782 | C | T | synonymous_variant | LOW | c.306G>A|p.Gln102Gln |
S87 |
8 | BAA10g02140 | A10 | 1016409 | G | A | upstream_gene_variant | MODIFIER | c.-322C>T| |
S289 |
9 | BAA10g02140 | A10 | 1016820 | C | T | upstream_gene_variant | MODIFIER | c.-733G>A| |
S298 |
10 | BAA10g02140 | A10 | 1018700 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S81 S85 |
11 | BAA10g02140 | A10 | 1019201 | G | A | upstream_gene_variant | MODIFIER | c.-3114C>T| |
S265 |
12 | BAA10g02140 | A10 | 1020004 | G | A | upstream_gene_variant | MODIFIER | c.-3917C>T| |
S205 |
13 | BAA10g02140 | A10 | 1020616 | C | T | upstream_gene_variant | MODIFIER | c.-4529G>A| |
S8 |
14 | BAA10g02140 | A10 | 1020856 | G | A | upstream_gene_variant | MODIFIER | c.-4769C>T| |
S290 |