Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15010 | A10 | 15561425 | C | T | missense_variant | MODERATE | c.3616G>A|p.Asp1206Asn |
S117 |
2 | BAA10g15010 | A10 | 15561911 | G | A | missense_variant | MODERATE | c.3130C>T|p.Pro1044Ser |
S236 |
3 | BAA10g15010 | A10 | 15563001 | C | T | missense_variant | MODERATE | c.2332G>A|p.Ala778Thr |
S297 |
4 | BAA10g15010 | A10 | 15563961 | G | A | synonymous_variant | LOW | c.1815C>T|p.Gly605Gly |
S32 |
5 | BAA10g15010 | A10 | 15567079 | G | A | synonymous_variant | LOW | c.457C>T|p.Leu153Leu |
S251 |
6 | BAA10g15010 | A10 | 15567199 | G | A | missense_variant | MODERATE | c.406C>T|p.Arg136Cys |
S139 |
7 | BAA10g15010 | A10 | 15567771 | G | A | upstream_gene_variant | MODIFIER | c.-93C>T| |
S264 |
8 | BAA10g15010 | A10 | 15570359 | C | T | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S230 |
9 | BAA10g15010 | A10 | 15571545 | G | A | upstream_gene_variant | MODIFIER | c.-3867C>T| |
S111 |
10 | BAA10g15010 | A10 | 15571850 | G | A | upstream_gene_variant | MODIFIER | c.-4172C>T| |
S288 |
11 | BAA10g15010 | A10 | 15572311 | G | A | upstream_gene_variant | MODIFIER | c.-4633C>T| |
S286 |