Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13980 | A10 | 14822507 | G | A | missense_variant | MODERATE | c.2864C>T|p.Ser955Leu |
S74 |
2 | BAA10g13980 | A10 | 14822988 | G | A | missense_variant | MODERATE | c.2383C>T|p.Pro795Ser |
S184 |
3 | BAA10g13980 | A10 | 14823294 | C | T | missense_variant | MODERATE | c.2077G>A|p.Val693Ile |
S249 |
4 | BAA10g13980 | A10 | 14823823 | C | T | synonymous_variant | LOW | c.1548G>A|p.Lys516Lys |
S79 S91 |
5 | BAA10g13980 | A10 | 14825806 | C | T | intron_variant | MODIFIER | c.125+51G>A| |
S103 |
6 | BAA10g13980 | A10 | 14825843 | G | A | intron_variant | MODIFIER | c.125+14C>T| |
S55 |
7 | BAA10g13980 | A10 | 14826059 | G | A | upstream_gene_variant | MODIFIER | c.-78C>T| |
S157 S166 S262 |
8 | BAA10g13980 | A10 | 14827291 | C | T | upstream_gene_variant | MODIFIER | c.-1310G>A| |
S277 |
9 | BAA10g13980 | A10 | 14828504 | G | A | upstream_gene_variant | MODIFIER | c.-2523C>T| |
S182 |
10 | BAA10g13980 | A10 | 14829379 | C | T | upstream_gene_variant | MODIFIER | c.-3398G>A| |
S168 |
11 | BAA10g13980 | A10 | 14830624 | C | T | upstream_gene_variant | MODIFIER | c.-4643G>A| |
S20 |