Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03280 | A01 | 1477785 | G | A | synonymous_variant | LOW | c.4809C>T|p.Cys1603Cys |
S9 |
2 | BAA01g03280 | A01 | 1478179 | C | T | synonymous_variant | LOW | c.4482G>A|p.Lys1494Lys |
S69 |
3 | BAA01g03280 | A01 | 1478566 | C | T | stop_gained | HIGH | c.4095G>A|p.Trp1365* |
S208 |
4 | BAA01g03280 | A01 | 1479585 | C | T | splice_region_variant&synonymous_variant | LOW | c.3498G>A|p.Thr1166Thr |
S71 |
5 | BAA01g03280 | A01 | 1479586 | G | A | missense_variant&splice_region_variant | MODERATE | c.3497C>T|p.Thr1166Met |
S219 |
6 | BAA01g03280 | A01 | 1479649 | C | T | missense_variant | MODERATE | c.3434G>A|p.Cys1145Tyr |
S94 |
7 | BAA01g03280 | A01 | 1479746 | G | A | synonymous_variant | LOW | c.3337C>T|p.Leu1113Leu |
S10 |
8 | BAA01g03280 | A01 | 1481223 | G | A | synonymous_variant | LOW | c.2379C>T|p.Phe793Phe |
S33 |
9 | BAA01g03280 | A01 | 1481240 | C | T | missense_variant | MODERATE | c.2362G>A|p.Asp788Asn |
S38 |
10 | BAA01g03280 | A01 | 1482854 | G | A | synonymous_variant | LOW | c.1059C>T|p.Ala353Ala |
S11 |
11 | BAA01g03280 | A01 | 1483290 | C | T | missense_variant | MODERATE | c.863G>A|p.Gly288Asp |
S30 S31 |
12 | BAA01g03280 | A01 | 1483321 | C | T | missense_variant | MODERATE | c.832G>A|p.Glu278Lys |
S25 |
13 | BAA01g03280 | A01 | 1483348 | G | A | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S294 |
14 | BAA01g03280 | A01 | 1483378 | G | A | stop_gained | HIGH | c.775C>T|p.Gln259* |
S256 |
15 | BAA01g03280 | A01 | 1483550 | C | T | synonymous_variant | LOW | c.603G>A|p.Ser201Ser |
S100 |
16 | BAA01g03280 | A01 | 1484565 | C | T | upstream_gene_variant | MODIFIER | c.-413G>A| |
S117 |
17 | BAA01g03280 | A01 | 1484870 | G | A | upstream_gene_variant | MODIFIER | c.-718C>T| |
S289 S290 |
18 | BAA01g03280 | A01 | 1488404 | G | A | upstream_gene_variant | MODIFIER | c.-4252C>T| |
S271 |