Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05800 | A08 | 4454741 | G | A | missense_variant | MODERATE | c.2189C>T|p.Thr730Ile |
S130 |
2 | BAA08g05800 | A08 | 4455394 | C | T | missense_variant | MODERATE | c.1619G>A|p.Arg540Lys |
S157 S163 |
3 | BAA08g05800 | A08 | 4455575 | C | T | missense_variant | MODERATE | c.1438G>A|p.Ala480Thr |
S78 S83 |
4 | BAA08g05800 | A08 | 4456231 | G | A | missense_variant | MODERATE | c.782C>T|p.Ser261Leu |
S223 |
5 | BAA08g05800 | A08 | 4456670 | C | T | missense_variant | MODERATE | c.343G>A|p.Glu115Lys |
S177 |
6 | BAA08g05800 | A08 | 4456671 | C | T | stop_gained | HIGH | c.342G>A|p.Trp114* |
S302 |
7 | BAA08g05800 | A08 | 4456758 | G | A | synonymous_variant | LOW | c.255C>T|p.Ile85Ile |
S238 |
8 | BAA08g05800 | A08 | 4456986 | C | T | synonymous_variant | LOW | c.27G>A|p.Glu9Glu |
S177 |
9 | BAA08g05800 | A08 | 4457008 | G | A | missense_variant | MODERATE | c.5C>T|p.Ser2Phe |
S241 |
10 | BAA08g05800 | A08 | 4457465 | C | T | upstream_gene_variant | MODIFIER | c.-453G>A| |
S25 |
11 | BAA08g05800 | A08 | 4457660 | C | T | upstream_gene_variant | MODIFIER | c.-648G>A| |
S66 |
12 | BAA08g05800 | A08 | 4458927 | G | A | upstream_gene_variant | MODIFIER | c.-1915C>T| |
S136 S55 |
13 | BAA08g05800 | A08 | 4459228 | G | A | upstream_gene_variant | MODIFIER | c.-2216C>T| |
S212 S259 |
14 | BAA08g05800 | A08 | 4461046 | G | A | upstream_gene_variant | MODIFIER | c.-4034C>T| |
S157 |
15 | BAA08g05800 | A08 | 4461204 | G | A | upstream_gene_variant | MODIFIER | c.-4192C>T| |
S69 |