Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10140 | A10 | 11879761 | C | T | upstream_gene_variant | MODIFIER | c.-3188C>T| |
S244 |
2 | BAA10g10140 | A10 | 11879959 | G | A | upstream_gene_variant | MODIFIER | c.-2990G>A| |
S148 S30 S31 |
3 | BAA10g10140 | A10 | 11880323 | T | G | upstream_gene_variant | MODIFIER | c.-2626T>G| |
S99 |
4 | BAA10g10140 | A10 | 11880771 | C | T | upstream_gene_variant | MODIFIER | c.-2178C>T| |
S37 |
5 | BAA10g10140 | A10 | 11880804 | G | A | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S240 |
6 | BAA10g10140 | A10 | 11881169 | G | A | upstream_gene_variant | MODIFIER | c.-1780G>A| |
S140 |
7 | BAA10g10140 | A10 | 11881731 | C | T | upstream_gene_variant | MODIFIER | c.-1218C>T| |
S152 |
8 | BAA10g10140 | A10 | 11882849 | C | T | upstream_gene_variant | MODIFIER | c.-100C>T| |
S297 |
9 | BAA10g10140 | A10 | 11884076 | G | A | synonymous_variant | LOW | c.1128G>A|p.Arg376Arg |
S107 |
10 | BAA10g10140 | A10 | 11884555 | C | T | missense_variant | MODERATE | c.1607C>T|p.Ser536Phe |
S224 |
11 | BAA10g10140 | A10 | 11885420 | C | T | downstream_gene_variant | MODIFIER | c.*144C>T| |
S166 |
12 | BAA10g10140 | A10 | 11885776 | G | A | downstream_gene_variant | MODIFIER | c.*500G>A| |
S64 |
13 | BAA10g10140 | A10 | 11886171 | C | T | downstream_gene_variant | MODIFIER | c.*895C>T| |
S305 |
14 | BAA10g10140 | A10 | 11886430 | C | T | downstream_gene_variant | MODIFIER | c.*1154C>T| |
S166 |
15 | BAA10g10140 | A10 | 11886450 | G | A | downstream_gene_variant | MODIFIER | c.*1174G>A| |
S111 |
16 | BAA10g10140 | A10 | 11887058 | G | A | downstream_gene_variant | MODIFIER | c.*1782G>A| |
S160 |
17 | BAA10g10140 | A10 | 11888357 | G | A | downstream_gene_variant | MODIFIER | c.*3081G>A| |
S198 |