Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11160 | A10 | 12808095 | G | A | upstream_gene_variant | MODIFIER | c.-4564G>A| |
S32 |
2 | BAA10g11160 | A10 | 12809096 | C | T | upstream_gene_variant | MODIFIER | c.-3563C>T| |
S270 |
3 | BAA10g11160 | A10 | 12809431 | G | A | upstream_gene_variant | MODIFIER | c.-3228G>A| |
S184 |
4 | BAA10g11160 | A10 | 12811735 | G | A | upstream_gene_variant | MODIFIER | c.-924G>A| |
S80 |
5 | BAA10g11160 | A10 | 12811895 | C | T | upstream_gene_variant | MODIFIER | c.-764C>T| |
S25 |
6 | BAA10g11160 | A10 | 12812048 | C | T | upstream_gene_variant | MODIFIER | c.-611C>T| |
S44 |
7 | BAA10g11160 | A10 | 12812664 | G | A | synonymous_variant | LOW | c.6G>A|p.Glu2Glu |
S71 |
8 | BAA10g11160 | A10 | 12813026 | G | A | missense_variant | MODERATE | c.368G>A|p.Arg123Lys |
S81 S85 |
9 | BAA10g11160 | A10 | 12813127 | G | A | missense_variant | MODERATE | c.469G>A|p.Glu157Lys |
S205 |
10 | BAA10g11160 | A10 | 12814020 | C | T | missense_variant | MODERATE | c.1202C>T|p.Pro401Leu |
S110 |
11 | BAA10g11160 | A10 | 12814196 | G | A | splice_donor_variant&intron_variant | HIGH | c.1377+1G>A| |
S262 |
12 | BAA10g11160 | A10 | 12814484 | C | T | missense_variant | MODERATE | c.1580C>T|p.Ala527Val |
S23 |
13 | BAA10g11160 | A10 | 12815096 | G | A | missense_variant | MODERATE | c.1843G>A|p.Gly615Ser |
S129 |