Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29600 | A10 | 22207056 | C | T | upstream_gene_variant | MODIFIER | c.-3503C>T| |
S86 |
2 | BAA10g29600 | A10 | 22207223 | C | T | upstream_gene_variant | MODIFIER | c.-3336C>T| |
S246 |
3 | BAA10g29600 | A10 | 22207873 | C | T | upstream_gene_variant | MODIFIER | c.-2686C>T| |
S301 S304 |
4 | BAA10g29600 | A10 | 22208479 | G | A | upstream_gene_variant | MODIFIER | c.-2080G>A| |
S125 |
5 | BAA10g29600 | A10 | 22208791 | G | A | upstream_gene_variant | MODIFIER | c.-1768G>A| |
S223 |
6 | BAA10g29600 | A10 | 22209189 | C | T | upstream_gene_variant | MODIFIER | c.-1370C>T| |
S112 |
7 | BAA10g29600 | A10 | 22210648 | G | A | synonymous_variant | LOW | c.90G>A|p.Glu30Glu |
S298 |
8 | BAA10g29600 | A10 | 22210707 | C | T | missense_variant | MODERATE | c.149C>T|p.Thr50Ile |
S259 |
9 | BAA10g29600 | A10 | 22210747 | G | A | synonymous_variant | LOW | c.189G>A|p.Gln63Gln |
S298 |
10 | BAA10g29600 | A10 | 22210826 | G | A | missense_variant | MODERATE | c.268G>A|p.Glu90Lys |
S251 |
11 | BAA10g29600 | A10 | 22211531 | G | A | missense_variant | MODERATE | c.728G>A|p.Gly243Glu |
S263 |
12 | BAA10g29600 | A10 | 22211703 | G | T | missense_variant | MODERATE | c.900G>T|p.Leu300Phe |
S197 |
13 | BAA10g29600 | A10 | 22212198 | C | T | synonymous_variant | LOW | c.1395C>T|p.Leu465Leu |
S92 |
14 | BAA10g29600 | A10 | 22217832 | G | A | downstream_gene_variant | MODIFIER | c.*1550G>A| |
S43 |