Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13190 | A10 | 14411310 | G | A | missense_variant | MODERATE | c.1552C>T|p.Leu518Phe |
S240 S287 |
2 | BAA10g13190 | A10 | 14411404 | C | T | synonymous_variant | LOW | c.1458G>A|p.Arg486Arg |
S12 |
3 | BAA10g13190 | A10 | 14411664 | C | T | missense_variant | MODERATE | c.1198G>A|p.Ala400Thr |
S86 |
4 | BAA10g13190 | A10 | 14411769 | C | T | missense_variant | MODERATE | c.1093G>A|p.Ala365Thr |
S96 |
5 | BAA10g13190 | A10 | 14411867 | G | A | missense_variant | MODERATE | c.995C>T|p.Ala332Val |
S221 |
6 | BAA10g13190 | A10 | 14412268 | G | A | synonymous_variant | LOW | c.670C>T|p.Leu224Leu |
S280 |
7 | BAA10g13190 | A10 | 14412487 | C | T | missense_variant | MODERATE | c.451G>A|p.Glu151Lys |
S131 |
8 | BAA10g13190 | A10 | 14412751 | C | T | missense_variant | MODERATE | c.187G>A|p.Gly63Arg |
S185 |
9 | BAA10g13190 | A10 | 14412958 | C | T | upstream_gene_variant | MODIFIER | c.-21G>A| |
S75 S81 |
10 | BAA10g13190 | A10 | 14413976 | C | T | upstream_gene_variant | MODIFIER | c.-1039G>A| |
S68 |
11 | BAA10g13190 | A10 | 14414328 | C | T | upstream_gene_variant | MODIFIER | c.-1391G>A| |
S44 |
12 | BAA10g13190 | A10 | 14416870 | G | A | upstream_gene_variant | MODIFIER | c.-3933C>T| |
S279 |
13 | BAA10g13190 | A10 | 14417388 | C | T | upstream_gene_variant | MODIFIER | c.-4451G>A| |
S46 |