Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29540 | A10 | 22183615 | C | T | upstream_gene_variant | MODIFIER | c.-748C>T| |
S262 |
2 | BAA10g29540 | A10 | 22184984 | C | T | missense_variant | MODERATE | c.148C>T|p.Pro50Ser |
S268 |
3 | BAA10g29540 | A10 | 22185642 | G | A | missense_variant | MODERATE | c.581G>A|p.Arg194Lys |
S298 |
4 | BAA10g29540 | A10 | 22185653 | G | A | missense_variant | MODERATE | c.592G>A|p.Glu198Lys |
S205 |
5 | BAA10g29540 | A10 | 22186701 | C | T | missense_variant | MODERATE | c.1640C>T|p.Ser547Phe |
S251 |
6 | BAA10g29540 | A10 | 22188221 | G | A | missense_variant | MODERATE | c.2677G>A|p.Ala893Thr |
S288 |
7 | BAA10g29540 | A10 | 22188243 | G | A | missense_variant | MODERATE | c.2699G>A|p.Cys900Tyr |
S239 |
8 | BAA10g29540 | A10 | 22188368 | C | T | missense_variant | MODERATE | c.2747C>T|p.Ser916Phe |
S48 |
9 | BAA10g29540 | A10 | 22188376 | C | T | missense_variant | MODERATE | c.2755C>T|p.Arg919Cys |
S176 |
10 | BAA10g29540 | A10 | 22189158 | C | T | stop_gained | HIGH | c.3442C>T|p.Gln1148* |
S247 |
11 | BAA10g29540 | A10 | 22190194 | C | T | downstream_gene_variant | MODIFIER | c.*39C>T| |
S40 S49 |
12 | BAA10g29540 | A10 | 22190935 | G | A | downstream_gene_variant | MODIFIER | c.*780G>A| |
S125 |
13 | BAA10g29540 | A10 | 22191192 | C | T | downstream_gene_variant | MODIFIER | c.*1037C>T| |
S302 |
14 | BAA10g29540 | A10 | 22191606 | G | A | downstream_gene_variant | MODIFIER | c.*1451G>A| |
S278 |