Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02950 | A06 | 1707824 | T | C | missense_variant | MODERATE | c.1784A>G|p.Glu595Gly |
S134 |
2 | BAA06g02950 | A06 | 1708016 | C | T | missense_variant | MODERATE | c.1592G>A|p.Gly531Glu |
S262 |
3 | BAA06g02950 | A06 | 1708055 | C | T | missense_variant | MODERATE | c.1553G>A|p.Gly518Glu |
S57 |
4 | BAA06g02950 | A06 | 1708356 | C | T | missense_variant | MODERATE | c.1336G>A|p.Gly446Arg |
S192 |
5 | BAA06g02950 | A06 | 1708697 | G | A | missense_variant | MODERATE | c.1250C>T|p.Ser417Phe |
S251 |
6 | BAA06g02950 | A06 | 1708916 | C | T | missense_variant | MODERATE | c.1102G>A|p.Ala368Thr |
S260 |
7 | BAA06g02950 | A06 | 1709318 | G | A | missense_variant | MODERATE | c.787C>T|p.Pro263Ser |
S178 |
8 | BAA06g02950 | A06 | 1709438 | G | A | missense_variant | MODERATE | c.667C>T|p.Arg223Trp |
S293 S294 |
9 | BAA06g02950 | A06 | 1709554 | C | T | missense_variant | MODERATE | c.551G>A|p.Cys184Tyr |
S55 |
10 | BAA06g02950 | A06 | 1709561 | C | T | missense_variant | MODERATE | c.544G>A|p.Val182Ile |
S70 |
11 | BAA06g02950 | A06 | 1709867 | C | T | intron_variant | MODIFIER | c.358-120G>A| |
S97 |
12 | BAA06g02950 | A06 | 1711415 | T | A | upstream_gene_variant | MODIFIER | c.-726A>T| |
S19 |
13 | BAA06g02950 | A06 | 1711694 | G | A | upstream_gene_variant | MODIFIER | c.-1005C>T| |
S182 |
14 | BAA06g02950 | A06 | 1713138 | C | G | upstream_gene_variant | MODIFIER | c.-2449G>C| |
S60 |