Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05490 | A10 | 2801850 | C | T | missense_variant | MODERATE | c.1282G>A|p.Asp428Asn |
S173 |
2 | BAA10g05490 | A10 | 2802008 | C | T | synonymous_variant | LOW | c.1209G>A|p.Glu403Glu |
S232 |
3 | BAA10g05490 | A10 | 2802292 | C | T | synonymous_variant | LOW | c.1014G>A|p.Arg338Arg |
S87 |
4 | BAA10g05490 | A10 | 2802786 | C | T | missense_variant | MODERATE | c.520G>A|p.Ala174Thr |
S152 |
5 | BAA10g05490 | A10 | 2804076 | C | T | missense_variant | MODERATE | c.34G>A|p.Asp12Asn |
S224 |
6 | BAA10g05490 | A10 | 2804250 | G | A | upstream_gene_variant | MODIFIER | c.-141C>T| |
S15 S3 |
7 | BAA10g05490 | A10 | 2804377 | G | A | upstream_gene_variant | MODIFIER | c.-268C>T| |
S283 |
8 | BAA10g05490 | A10 | 2804599 | G | A | upstream_gene_variant | MODIFIER | c.-490C>T| |
S261 |
9 | BAA10g05490 | A10 | 2805394 | C | T | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S244 |
10 | BAA10g05490 | A10 | 2806298 | C | T | upstream_gene_variant | MODIFIER | c.-2189G>A| |
S10 |
11 | BAA10g05490 | A10 | 2809045 | C | T | upstream_gene_variant | MODIFIER | c.-4936G>A| |
S135 |