Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08350 | A10 | 10078952 | G | A | downstream_gene_variant | MODIFIER | c.*3456C>T| |
S206 |
2 | BAA10g08350 | A10 | 10079131 | C | T | downstream_gene_variant | MODIFIER | c.*3277G>A| |
S193 |
3 | BAA10g08350 | A10 | 10079325 | G | A | downstream_gene_variant | MODIFIER | c.*3083C>T| |
S18 |
4 | BAA10g08350 | A10 | 10079934 | G | A | downstream_gene_variant | MODIFIER | c.*2474C>T| |
S66 |
5 | BAA10g08350 | A10 | 10080617 | C | T | downstream_gene_variant | MODIFIER | c.*1791G>A| |
S68 |
6 | BAA10g08350 | A10 | 10081392 | G | A | downstream_gene_variant | MODIFIER | c.*1016C>T| |
S251 |
7 | BAA10g08350 | A10 | 10082342 | G | A | downstream_gene_variant | MODIFIER | c.*66C>T| |
S15 S3 |
8 | BAA10g08350 | A10 | 10082760 | C | T | missense_variant | MODERATE | c.1052G>A|p.Gly351Glu |
S25 |
9 | BAA10g08350 | A10 | 10083711 | C | T | intron_variant | MODIFIER | c.902-801G>A| |
S270 |
10 | BAA10g08350 | A10 | 10083987 | C | T | intron_variant | MODIFIER | c.902-1077G>A| |
S169 |
11 | BAA10g08350 | A10 | 10084127 | G | A | intron_variant | MODIFIER | c.902-1217C>T| |
S234 |
12 | BAA10g08350 | A10 | 10084569 | C | T | intron_variant | MODIFIER | c.901+867G>A| |
S144 |
13 | BAA10g08350 | A10 | 10085481 | G | A | missense_variant | MODERATE | c.856C>T|p.Pro286Ser |
S221 |
14 | BAA10g08350 | A10 | 10085865 | C | T | missense_variant | MODERATE | c.472G>A|p.Val158Ile |
S188 S265 |
15 | BAA10g08350 | A10 | 10086204 | G | A | missense_variant | MODERATE | c.133C>T|p.Pro45Ser |
S172 S217 |