Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05100 | A10 | 2621187 | C | T | missense_variant | MODERATE | c.1678G>A|p.Glu560Lys |
S181 |
2 | BAA10g05100 | A10 | 2622371 | C | T | missense_variant | MODERATE | c.799G>A|p.Asp267Asn |
S44 |
3 | BAA10g05100 | A10 | 2622476 | C | T | missense_variant | MODERATE | c.694G>A|p.Gly232Arg |
S210 |
4 | BAA10g05100 | A10 | 2622989 | G | A | missense_variant | MODERATE | c.218C>T|p.Ala73Val |
S83 |
5 | BAA10g05100 | A10 | 2623153 | C | T | missense_variant | MODERATE | c.54G>A|p.Met18Ile |
S135 |
6 | BAA10g05100 | A10 | 2623971 | G | A | upstream_gene_variant | MODIFIER | c.-765C>T| |
S240 |
7 | BAA10g05100 | A10 | 2624856 | G | A | upstream_gene_variant | MODIFIER | c.-1650C>T| |
S242 |
8 | BAA10g05100 | A10 | 2625017 | C | T | upstream_gene_variant | MODIFIER | c.-1811G>A| |
S2 |
9 | BAA10g05100 | A10 | 2625527 | G | A | upstream_gene_variant | MODIFIER | c.-2321C>T| |
S296 |
10 | BAA10g05100 | A10 | 2627854 | C | T | upstream_gene_variant | MODIFIER | c.-4648G>A| |
S204 |