Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g27810 | A06 | 19111127 | C | T | downstream_gene_variant | MODIFIER | c.*1692G>A| |
S267 |
2 | BAA06g27810 | A06 | 19112848 | C | T | missense_variant | MODERATE | c.1384G>A|p.Glu462Lys |
S138 S237 S288 |
3 | BAA06g27810 | A06 | 19112894 | G | A | splice_region_variant&intron_variant | LOW | c.1344-6C>T| |
S166 |
4 | BAA06g27810 | A06 | 19113442 | C | T | missense_variant | MODERATE | c.1111G>A|p.Glu371Lys |
S282 |
5 | BAA06g27810 | A06 | 19113788 | G | A | synonymous_variant | LOW | c.858C>T|p.Asn286Asn |
S139 |
6 | BAA06g27810 | A06 | 19114522 | G | A | missense_variant | MODERATE | c.419C>T|p.Ala140Val |
S11 |
7 | BAA06g27810 | A06 | 19114564 | C | T | missense_variant | MODERATE | c.377G>A|p.Gly126Glu |
S247 |
8 | BAA06g27810 | A06 | 19114737 | G | A | synonymous_variant | LOW | c.204C>T|p.Leu68Leu |
S28 |
9 | BAA06g27810 | A06 | 19114806 | G | A | synonymous_variant | LOW | c.135C>T|p.Ile45Ile |
S89 |
10 | BAA06g27810 | A06 | 19115057 | G | A | upstream_gene_variant | MODIFIER | c.-117C>T| |
S256 |
11 | BAA06g27810 | A06 | 19115563 | C | T | upstream_gene_variant | MODIFIER | c.-623G>A| |
S247 |
12 | BAA06g27810 | A06 | 19115682 | C | T | upstream_gene_variant | MODIFIER | c.-742G>A| |
S272 |
13 | BAA06g27810 | A06 | 19115822 | C | T | upstream_gene_variant | MODIFIER | c.-882G>A| |
S14 |
14 | BAA06g27810 | A06 | 19116531 | G | A | upstream_gene_variant | MODIFIER | c.-1591C>T| |
S74 |
15 | BAA06g27810 | A06 | 19116664 | G | A | upstream_gene_variant | MODIFIER | c.-1724C>T| |
S17 |
16 | BAA06g27810 | A06 | 19117278 | C | T | upstream_gene_variant | MODIFIER | c.-2338G>A| |
S148 S30 S31 |
17 | BAA06g27810 | A06 | 19117496 | G | A | upstream_gene_variant | MODIFIER | c.-2556C>T| |
S19 |
18 | BAA06g27810 | A06 | 19118965 | C | T | upstream_gene_variant | MODIFIER | c.-4025G>A| |
S153 |
19 | BAA06g27810 | A06 | 19119336 | G | A | upstream_gene_variant | MODIFIER | c.-4396C>T| |
S28 |