Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06750 | A10 | 3616582 | G | A | missense_variant | MODERATE | c.256G>A|p.Glu86Lys |
S167 |
2 | BAA10g06750 | A10 | 3617392 | C | T | missense_variant | MODERATE | c.1066C>T|p.Pro356Ser |
S298 |
3 | BAA10g06750 | A10 | 3617503 | G | A | missense_variant | MODERATE | c.1177G>A|p.Asp393Asn |
S226 |
4 | BAA10g06750 | A10 | 3617527 | G | A | missense_variant | MODERATE | c.1201G>A|p.Gly401Arg |
S18 |
5 | BAA10g06750 | A10 | 3617956 | G | A | missense_variant | MODERATE | c.1630G>A|p.Glu544Lys |
S105 S106 |
6 | BAA10g06750 | A10 | 3618001 | G | A | missense_variant | MODERATE | c.1675G>A|p.Glu559Lys |
S274 |
7 | BAA10g06750 | A10 | 3618170 | A | C | missense_variant | MODERATE | c.1844A>C|p.Lys615Thr |
S137 S167 S201 S296 S299 S308 S62 |
8 | BAA10g06750 | A10 | 3618613 | G | A | downstream_gene_variant | MODIFIER | c.*403G>A| |
S66 |
9 | BAA10g06750 | A10 | 3619392 | G | A | downstream_gene_variant | MODIFIER | c.*1182G>A| |
S209 |
10 | BAA10g06750 | A10 | 3620082 | G | A | downstream_gene_variant | MODIFIER | c.*1872G>A| |
S230 |
11 | BAA10g06750 | A10 | 3620222 | G | A | downstream_gene_variant | MODIFIER | c.*2012G>A| |
S48 |
12 | BAA10g06750 | A10 | 3620410 | G | A | downstream_gene_variant | MODIFIER | c.*2200G>A| |
S262 |
13 | BAA10g06750 | A10 | 3621147 | G | A | downstream_gene_variant | MODIFIER | c.*2937G>A| |
S20 |
14 | BAA10g06750 | A10 | 3623028 | G | A | downstream_gene_variant | MODIFIER | c.*4818G>A| |
S261 |