Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06910 | A10 | 3695071 | C | T | missense_variant | MODERATE | c.2428G>A|p.Ala810Thr |
S95 |
2 | BAA10g06910 | A10 | 3695403 | G | A | missense_variant | MODERATE | c.2096C>T|p.Pro699Leu |
S192 |
3 | BAA10g06910 | A10 | 3695653 | C | T | missense_variant | MODERATE | c.1846G>A|p.Glu616Lys |
S195 |
4 | BAA10g06910 | A10 | 3696261 | G | A | missense_variant | MODERATE | c.1646C>T|p.Ala549Val |
S39 |
5 | BAA10g06910 | A10 | 3696464 | C | T | synonymous_variant | LOW | c.1443G>A|p.Lys481Lys |
S256 S259 |
6 | BAA10g06910 | A10 | 3696556 | G | A | stop_gained | HIGH | c.1351C>T|p.Gln451* |
S13 |
7 | BAA10g06910 | A10 | 3696935 | C | T | synonymous_variant | LOW | c.972G>A|p.Pro324Pro |
S14 S272 |
8 | BAA10g06910 | A10 | 3697467 | C | T | missense_variant | MODERATE | c.551G>A|p.Gly184Glu |
S288 |
9 | BAA10g06910 | A10 | 3697987 | G | A | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S33 |
10 | BAA10g06910 | A10 | 3698783 | C | T | upstream_gene_variant | MODIFIER | c.-766G>A| |
S139 S249 |
11 | BAA10g06910 | A10 | 3699459 | G | A | upstream_gene_variant | MODIFIER | c.-1442C>T| |
S25 |
12 | BAA10g06910 | A10 | 3699803 | G | A | upstream_gene_variant | MODIFIER | c.-1786C>T| |
S198 |
13 | BAA10g06910 | A10 | 3699907 | C | T | upstream_gene_variant | MODIFIER | c.-1890G>A| |
S308 |
14 | BAA10g06910 | A10 | 3700334 | G | A | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S192 |
15 | BAA10g06910 | A10 | 3700462 | C | T | upstream_gene_variant | MODIFIER | c.-2445G>A| |
S143 |
16 | BAA10g06910 | A10 | 3700801 | C | T | upstream_gene_variant | MODIFIER | c.-2784G>A| |
S246 |
17 | BAA10g06910 | A10 | 3701570 | C | T | upstream_gene_variant | MODIFIER | c.-3553G>A| |
S116 |
18 | BAA10g06910 | A10 | 3701941 | G | A | upstream_gene_variant | MODIFIER | c.-3924C>T| |
S62 |
19 | BAA10g06910 | A10 | 3702691 | G | A | upstream_gene_variant | MODIFIER | c.-4674C>T| |
S105 S106 |
20 | BAA10g06910 | A10 | 3702865 | G | A | upstream_gene_variant | MODIFIER | c.-4848C>T| |
S53 |