Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g22850 | A06 | 12779627 | G | A | downstream_gene_variant | MODIFIER | c.*4868C>T| |
S173 |
2 | BAA06g22850 | A06 | 12780414 | G | A | downstream_gene_variant | MODIFIER | c.*4081C>T| |
S173 |
3 | BAA06g22850 | A06 | 12780517 | G | A | downstream_gene_variant | MODIFIER | c.*3978C>T| |
S139 |
4 | BAA06g22850 | A06 | 12782077 | C | T | downstream_gene_variant | MODIFIER | c.*2418G>A| |
S225 |
5 | BAA06g22850 | A06 | 12784809 | C | T | missense_variant | MODERATE | c.2422G>A|p.Asp808Asn |
S282 |
6 | BAA06g22850 | A06 | 12785244 | G | A | missense_variant | MODERATE | c.1987C>T|p.Pro663Ser |
S297 |
7 | BAA06g22850 | A06 | 12785543 | G | A | missense_variant | MODERATE | c.1688C>T|p.Ser563Phe |
S150 |
8 | BAA06g22850 | A06 | 12786948 | G | A | intron_variant | MODIFIER | c.628-26C>T| |
S1 |
9 | BAA06g22850 | A06 | 12787541 | C | T | intron_variant | MODIFIER | c.495+55G>A| |
S286 |
10 | BAA06g22850 | A06 | 12788652 | G | A | missense_variant | MODERATE | c.65C>T|p.Ala22Val |
S216 |
11 | BAA06g22850 | A06 | 12789483 | C | T | upstream_gene_variant | MODIFIER | c.-767G>A| |
S15 S3 |
12 | BAA06g22850 | A06 | 12789626 | C | T | upstream_gene_variant | MODIFIER | c.-910G>A| |
S148 S210 S30 S31 |
13 | BAA06g22850 | A06 | 12789975 | C | T | upstream_gene_variant | MODIFIER | c.-1259G>A| |
S179 |
14 | BAA06g22850 | A06 | 12790440 | C | A | upstream_gene_variant | MODIFIER | c.-1724G>T| |
S168 |
15 | BAA06g22850 | A06 | 12790606 | G | A | upstream_gene_variant | MODIFIER | c.-1890C>T| |
S166 |
16 | BAA06g22850 | A06 | 12791539 | G | A | upstream_gene_variant | MODIFIER | c.-2823C>T| |
S138 |