Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14020 | A10 | 14876517 | G | A | upstream_gene_variant | MODIFIER | c.-4470G>A| |
S121 |
2 | BAA10g14020 | A10 | 14876659 | C | T | upstream_gene_variant | MODIFIER | c.-4328C>T| |
S19 |
3 | BAA10g14020 | A10 | 14877069 | G | A | upstream_gene_variant | MODIFIER | c.-3918G>A| |
S265 |
4 | BAA10g14020 | A10 | 14878489 | G | A | upstream_gene_variant | MODIFIER | c.-2498G>A| |
S295 |
5 | BAA10g14020 | A10 | 14879734 | G | A | upstream_gene_variant | MODIFIER | c.-1253G>A| |
S201 |
6 | BAA10g14020 | A10 | 14879783 | G | A | upstream_gene_variant | MODIFIER | c.-1204G>A| |
S283 |
7 | BAA10g14020 | A10 | 14880879 | C | T | upstream_gene_variant | MODIFIER | c.-108C>T| |
S177 |
8 | BAA10g14020 | A10 | 14881304 | G | A | missense_variant | MODERATE | c.318G>A|p.Met106Ile |
S67 |
9 | BAA10g14020 | A10 | 14881380 | C | T | missense_variant | MODERATE | c.394C>T|p.Pro132Ser |
S56 |
10 | BAA10g14020 | A10 | 14881707 | C | T | synonymous_variant | LOW | c.639C>T|p.Ser213Ser |
S135 |
11 | BAA10g14020 | A10 | 14882155 | G | A | missense_variant | MODERATE | c.1087G>A|p.Glu363Lys |
S293 |
12 | BAA10g14020 | A10 | 14882360 | G | A | missense_variant | MODERATE | c.1292G>A|p.Gly431Asp |
S43 |
13 | BAA10g14020 | A10 | 14883919 | C | T | downstream_gene_variant | MODIFIER | c.*667C>T| |
S80 |
14 | BAA10g14020 | A10 | 14884112 | G | A | downstream_gene_variant | MODIFIER | c.*860G>A| |
S167 |