Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06040 | A10 | 3110068 | C | T | missense_variant | MODERATE | c.1336G>A|p.Ala446Thr |
S143 |
2 | BAA10g06040 | A10 | 3111009 | G | A | missense_variant | MODERATE | c.673C>T|p.Pro225Ser |
S292 |
3 | BAA10g06040 | A10 | 3111396 | G | A | splice_region_variant&intron_variant | LOW | c.350+8C>T| |
S278 |
4 | BAA10g06040 | A10 | 3112490 | C | T | upstream_gene_variant | MODIFIER | c.-397G>A| |
S260 |
5 | BAA10g06040 | A10 | 3113116 | C | T | upstream_gene_variant | MODIFIER | c.-1023G>A| |
S272 |
6 | BAA10g06040 | A10 | 3115695 | G | A | upstream_gene_variant | MODIFIER | c.-3602C>T| |
S212 |
7 | BAA10g06040 | A10 | 3115857 | G | A | upstream_gene_variant | MODIFIER | c.-3764C>T| |
S278 |
8 | BAA10g06040 | A10 | 3116385 | C | T | upstream_gene_variant | MODIFIER | c.-4292G>A| |
|
9 | BAA10g06040 | A10 | 3116819 | G | A | upstream_gene_variant | MODIFIER | c.-4726C>T| |
S158 |
10 | BAA10g06040 | A10 | 3116974 | A | C | upstream_gene_variant | MODIFIER | c.-4881T>G| |
S116 S215 S228 S252 S275 |
11 | BAA10g06040 | A10 | 3117079 | C | T | upstream_gene_variant | MODIFIER | c.-4986G>A| |
S144 |