Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23880 | A10 | 19899502 | C | T | upstream_gene_variant | MODIFIER | c.-2345C>T| |
S153 S213 |
2 | BAA10g23880 | A10 | 19899762 | G | A | upstream_gene_variant | MODIFIER | c.-2085G>A| |
S278 |
3 | BAA10g23880 | A10 | 19899956 | C | T | upstream_gene_variant | MODIFIER | c.-1891C>T| |
S203 |
4 | BAA10g23880 | A10 | 19901976 | G | A | missense_variant | MODERATE | c.130G>A|p.Val44Ile |
S159 S243 |
5 | BAA10g23880 | A10 | 19901984 | C | T | synonymous_variant | LOW | c.138C>T|p.Tyr46Tyr |
S122 |
6 | BAA10g23880 | A10 | 19902498 | C | T | missense_variant | MODERATE | c.386C>T|p.Ala129Val |
S46 |
7 | BAA10g23880 | A10 | 19904075 | C | T | synonymous_variant | LOW | c.1098C>T|p.Phe366Phe |
S26 |
8 | BAA10g23880 | A10 | 19904091 | C | T | missense_variant | MODERATE | c.1114C>T|p.Pro372Ser |
S5 |
9 | BAA10g23880 | A10 | 19904151 | C | T | missense_variant | MODERATE | c.1174C>T|p.Pro392Ser |
S68 |
10 | BAA10g23880 | A10 | 19904582 | C | T | synonymous_variant | LOW | c.1425C>T|p.Tyr475Tyr |
S209 |