Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19140 | A08 | 15150182 | C | T | missense_variant | MODERATE | c.1900G>A|p.Glu634Lys |
S280 |
2 | BAA08g19140 | A08 | 15150468 | C | T | synonymous_variant | LOW | c.1614G>A|p.Lys538Lys |
S121 |
3 | BAA08g19140 | A08 | 15150611 | C | T | missense_variant | MODERATE | c.1471G>A|p.Gly491Arg |
S69 |
4 | BAA08g19140 | A08 | 15150938 | C | T | missense_variant | MODERATE | c.1144G>A|p.Asp382Asn |
S180 |
5 | BAA08g19140 | A08 | 15151889 | G | A | intron_variant | MODIFIER | c.442+201C>T| |
S65 |
6 | BAA08g19140 | A08 | 15152130 | G | A | synonymous_variant | LOW | c.402C>T|p.Phe134Phe |
S274 |
7 | BAA08g19140 | A08 | 15152919 | G | A | upstream_gene_variant | MODIFIER | c.-312C>T| |
S42 |
8 | BAA08g19140 | A08 | 15153560 | G | A | upstream_gene_variant | MODIFIER | c.-953C>T| |
S10 |
9 | BAA08g19140 | A08 | 15154400 | G | A | upstream_gene_variant | MODIFIER | c.-1793C>T| |
S266 |
10 | BAA08g19140 | A08 | 15155552 | C | T | upstream_gene_variant | MODIFIER | c.-2945G>A| |
S60 |
11 | BAA08g19140 | A08 | 15155584 | C | T | upstream_gene_variant | MODIFIER | c.-2977G>A| |
S67 |
12 | BAA08g19140 | A08 | 15155630 | G | A | upstream_gene_variant | MODIFIER | c.-3023C>T| |
S302 |
13 | BAA08g19140 | A08 | 15157218 | G | A | upstream_gene_variant | MODIFIER | c.-4611C>T| |
S35 |