Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06250 | A01 | 2794716 | C | T | missense_variant | MODERATE | c.2104G>A|p.Glu702Lys |
S244 |
2 | BAA01g06250 | A01 | 2794888 | G | A | synonymous_variant | LOW | c.1932C>T|p.Phe644Phe |
S192 |
3 | BAA01g06250 | A01 | 2795681 | C | T | missense_variant | MODERATE | c.1480G>A|p.Glu494Lys |
S284 |
4 | BAA01g06250 | A01 | 2796327 | C | T | missense_variant | MODERATE | c.1075G>A|p.Asp359Asn |
S231 |
5 | BAA01g06250 | A01 | 2796359 | C | T | missense_variant | MODERATE | c.1043G>A|p.Gly348Asp |
S51 |
6 | BAA01g06250 | A01 | 2796558 | G | A | stop_gained | HIGH | c.844C>T|p.Arg282* |
S142 |
7 | BAA01g06250 | A01 | 2797071 | C | T | synonymous_variant | LOW | c.417G>A|p.Thr139Thr |
S296 |
8 | BAA01g06250 | A01 | 2797991 | C | T | missense_variant | MODERATE | c.100G>A|p.Asp34Asn |
S144 |
9 | BAA01g06250 | A01 | 2798483 | C | T | upstream_gene_variant | MODIFIER | c.-42G>A| |
S89 |
10 | BAA01g06250 | A01 | 2798569 | G | A | upstream_gene_variant | MODIFIER | c.-128C>T| |
S229 |
11 | BAA01g06250 | A01 | 2799008 | C | T | upstream_gene_variant | MODIFIER | c.-567G>A| |
S1 S90 |
12 | BAA01g06250 | A01 | 2800189 | C | T | upstream_gene_variant | MODIFIER | c.-1748G>A| |
S171 |
13 | BAA01g06250 | A01 | 2800630 | C | T | upstream_gene_variant | MODIFIER | c.-2189G>A| |
S275 |
14 | BAA01g06250 | A01 | 2800986 | C | T | upstream_gene_variant | MODIFIER | c.-2545G>A| |
S38 |
15 | BAA01g06250 | A01 | 2802095 | G | A | upstream_gene_variant | MODIFIER | c.-3654C>T| |
S121 |