Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g04580 | A06 | 2604349 | G | A | missense_variant | MODERATE | c.1969C>T|p.Arg657Cys |
S62 |
2 | BAA06g04580 | A06 | 2605612 | C | T | missense_variant | MODERATE | c.1201G>A|p.Glu401Lys |
S38 |
3 | BAA06g04580 | A06 | 2606856 | G | A | missense_variant | MODERATE | c.532C>T|p.Pro178Ser |
S196 |
4 | BAA06g04580 | A06 | 2606942 | G | A | missense_variant | MODERATE | c.446C>T|p.Ala149Val |
S261 |
5 | BAA06g04580 | A06 | 2606975 | G | A | missense_variant | MODERATE | c.413C>T|p.Ala138Val |
S280 |
6 | BAA06g04580 | A06 | 2607115 | C | T | missense_variant | MODERATE | c.367G>A|p.Asp123Asn |
S18 |
7 | BAA06g04580 | A06 | 2607481 | G | A | missense_variant | MODERATE | c.212C>T|p.Ser71Phe |
S208 S219 |
8 | BAA06g04580 | A06 | 2608589 | G | A | upstream_gene_variant | MODIFIER | c.-599C>T| |
S149 |
9 | BAA06g04580 | A06 | 2608940 | C | T | upstream_gene_variant | MODIFIER | c.-950G>A| |
S162 |
10 | BAA06g04580 | A06 | 2611112 | G | A | upstream_gene_variant | MODIFIER | c.-3122C>T| |
S168 |
11 | BAA06g04580 | A06 | 2611485 | C | T | upstream_gene_variant | MODIFIER | c.-3495G>A| |
S120 |
12 | BAA06g04580 | A06 | 2611774 | C | T | upstream_gene_variant | MODIFIER | c.-3784G>A| |
S185 |