Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g00570 | A03 | 211411 | G | A | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S149 |
2 | BAA03g00570 | A03 | 213003 | C | T | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S59 |
3 | BAA03g00570 | A03 | 213951 | G | A | upstream_gene_variant | MODIFIER | c.-2066G>A| |
S294 |
4 | BAA03g00570 | A03 | 214180 | C | T | upstream_gene_variant | MODIFIER | c.-1837C>T| |
S233 |
5 | BAA03g00570 | A03 | 214438 | C | T | upstream_gene_variant | MODIFIER | c.-1579C>T| |
S230 |
6 | BAA03g00570 | A03 | 214980 | G | A | upstream_gene_variant | MODIFIER | c.-1037G>A| |
S286 |
7 | BAA03g00570 | A03 | 215126 | G | A | upstream_gene_variant | MODIFIER | c.-891G>A| |
S123 |
8 | BAA03g00570 | A03 | 216065 | G | A | missense_variant | MODERATE | c.49G>A|p.Asp17Asn |
S10 |
9 | BAA03g00570 | A03 | 216453 | C | T | missense_variant | MODERATE | c.437C>T|p.Ala146Val |
S82 S92 |
10 | BAA03g00570 | A03 | 217736 | G | A | missense_variant | MODERATE | c.946G>A|p.Asp316Asn |
S118 S119 |
11 | BAA03g00570 | A03 | 217843 | G | A | stop_gained | HIGH | c.1053G>A|p.Trp351* |
S287 |
12 | BAA03g00570 | A03 | 219035 | G | A | missense_variant | MODERATE | c.1427G>A|p.Gly476Glu |
S274 |
13 | BAA03g00570 | A03 | 219321 | G | A | downstream_gene_variant | MODIFIER | c.*15G>A| |
S272 |
14 | BAA03g00570 | A03 | 220585 | C | T | downstream_gene_variant | MODIFIER | c.*1279C>T| |
S199 |
15 | BAA03g00570 | A03 | 220728 | G | A | downstream_gene_variant | MODIFIER | c.*1422G>A| |
S246 |
16 | BAA03g00570 | A03 | 220937 | C | T | downstream_gene_variant | MODIFIER | c.*1631C>T| |
S8 |