Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19700 | A06 | 10222589 | C | T | downstream_gene_variant | MODIFIER | c.*2411G>A| |
S199 |
2 | BAA06g19700 | A06 | 10225348 | C | T | synonymous_variant | LOW | c.3147G>A|p.Leu1049Leu |
S260 |
3 | BAA06g19700 | A06 | 10225540 | G | A | synonymous_variant | LOW | c.2955C>T|p.Cys985Cys |
S272 |
4 | BAA06g19700 | A06 | 10226748 | A | G | missense_variant | MODERATE | c.2630T>C|p.Leu877Pro |
S124 S126 S127 S128 S131 S223 S284 S286 S287 S57 S61 |
5 | BAA06g19700 | A06 | 10227005 | G | A | synonymous_variant | LOW | c.2373C>T|p.Leu791Leu |
S185 |
6 | BAA06g19700 | A06 | 10227170 | C | T | synonymous_variant | LOW | c.2208G>A|p.Thr736Thr |
S249 |
7 | BAA06g19700 | A06 | 10227408 | C | T | stop_gained | HIGH | c.1970G>A|p.Trp657* |
S108 S4 |
8 | BAA06g19700 | A06 | 10227550 | G | A | missense_variant | MODERATE | c.1828C>T|p.Leu610Phe |
S237 S288 |
9 | BAA06g19700 | A06 | 10227733 | G | A | missense_variant | MODERATE | c.1645C>T|p.Leu549Phe |
S138 |
10 | BAA06g19700 | A06 | 10228534 | G | A | missense_variant | MODERATE | c.1015C>T|p.Leu339Phe |
S9 |
11 | BAA06g19700 | A06 | 10228545 | C | G | missense_variant | MODERATE | c.1004G>C|p.Cys335Ser |
S162 |
12 | BAA06g19700 | A06 | 10231713 | G | A | missense_variant | MODERATE | c.56C>T|p.Ala19Val |
S3 |
13 | BAA06g19700 | A06 | 10235226 | G | A | upstream_gene_variant | MODIFIER | c.-3458C>T| |
S244 |
14 | BAA06g19700 | A06 | 10235413 | G | A | upstream_gene_variant | MODIFIER | c.-3645C>T| |
S143 |