Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10060 | A10 | 11842416 | C | T | upstream_gene_variant | MODIFIER | c.-3950C>T| |
S19 |
2 | BAA10g10060 | A10 | 11842439 | C | T | upstream_gene_variant | MODIFIER | c.-3927C>T| |
S17 |
3 | BAA10g10060 | A10 | 11842446 | C | T | upstream_gene_variant | MODIFIER | c.-3920C>T| |
S61 |
4 | BAA10g10060 | A10 | 11842554 | C | T | upstream_gene_variant | MODIFIER | c.-3812C>T| |
S99 |
5 | BAA10g10060 | A10 | 11842997 | G | A | upstream_gene_variant | MODIFIER | c.-3369G>A| |
S48 |
6 | BAA10g10060 | A10 | 11843515 | C | T | upstream_gene_variant | MODIFIER | c.-2851C>T| |
S146 |
7 | BAA10g10060 | A10 | 11844084 | C | T | upstream_gene_variant | MODIFIER | c.-2282C>T| |
S225 S73 |
8 | BAA10g10060 | A10 | 11846488 | C | T | synonymous_variant | LOW | c.123C>T|p.Thr41Thr |
S117 |
9 | BAA10g10060 | A10 | 11846501 | C | T | missense_variant | MODERATE | c.136C>T|p.Pro46Ser |
S171 |
10 | BAA10g10060 | A10 | 11847111 | C | T | missense_variant | MODERATE | c.746C>T|p.Ser249Phe |
S53 S81 S82 S85 S92 |
11 | BAA10g10060 | A10 | 11847576 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S34 |