Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g09170 | A06 | 4686296 | C | T | missense_variant | MODERATE | c.1705G>A|p.Asp569Asn |
S60 |
2 | BAA06g09170 | A06 | 4686614 | C | T | missense_variant | MODERATE | c.1387G>A|p.Gly463Arg |
S144 |
3 | BAA06g09170 | A06 | 4686750 | G | A | synonymous_variant | LOW | c.1251C>T|p.Pro417Pro |
S273 S54 |
4 | BAA06g09170 | A06 | 4686763 | C | T | missense_variant | MODERATE | c.1238G>A|p.Gly413Asp |
S232 |
5 | BAA06g09170 | A06 | 4687151 | C | T | missense_variant | MODERATE | c.850G>A|p.Gly284Arg |
S308 |
6 | BAA06g09170 | A06 | 4687474 | G | A | missense_variant | MODERATE | c.527C>T|p.Thr176Met |
S38 |
7 | BAA06g09170 | A06 | 4689011 | C | T | upstream_gene_variant | MODIFIER | c.-1011G>A| |
S11 |
8 | BAA06g09170 | A06 | 4691140 | C | T | upstream_gene_variant | MODIFIER | c.-3140G>A| |
S230 |
9 | BAA06g09170 | A06 | 4691499 | G | A | upstream_gene_variant | MODIFIER | c.-3499C>T| |
S152 |
10 | BAA06g09170 | A06 | 4691930 | C | T | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S6 |
11 | BAA06g09170 | A06 | 4692975 | C | T | upstream_gene_variant | MODIFIER | c.-4975G>A| |
S57 |