Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13990 | A01 | 6651493 | A | G | upstream_gene_variant | MODIFIER | c.-4861A>G| |
S115 |
2 | BAA01g13990 | A01 | 6656501 | G | A | missense_variant | MODERATE | c.148G>A|p.Val50Met |
S129 |
3 | BAA01g13990 | A01 | 6656933 | C | T | synonymous_variant | LOW | c.492C>T|p.Gly164Gly |
S80 |
4 | BAA01g13990 | A01 | 6657702 | G | A | missense_variant | MODERATE | c.1261G>A|p.Gly421Ser |
S105 S106 |
5 | BAA01g13990 | A01 | 6658000 | C | T | missense_variant | MODERATE | c.1492C>T|p.His498Tyr |
S249 |
6 | BAA01g13990 | A01 | 6659019 | G | A | synonymous_variant | LOW | c.2511G>A|p.Arg837Arg |
S122 |
7 | BAA01g13990 | A01 | 6659224 | G | A | missense_variant | MODERATE | c.2716G>A|p.Asp906Asn |
S8 |
8 | BAA01g13990 | A01 | 6659341 | G | A | missense_variant | MODERATE | c.2833G>A|p.Asp945Asn |
S110 |
9 | BAA01g13990 | A01 | 6659367 | C | T | synonymous_variant | LOW | c.2859C>T|p.Phe953Phe |
S226 |
10 | BAA01g13990 | A01 | 6659630 | C | T | missense_variant | MODERATE | c.3122C>T|p.Ser1041Phe |
S158 |
11 | BAA01g13990 | A01 | 6661470 | C | T | synonymous_variant | LOW | c.3579C>T|p.Arg1193Arg |
S2 |
12 | BAA01g13990 | A01 | 6661509 | T | C | synonymous_variant | LOW | c.3618T>C|p.Arg1206Arg |
S235 |
13 | BAA01g13990 | A01 | 6661542 | C | T | synonymous_variant | LOW | c.3651C>T|p.Leu1217Leu |
S132 S137 |
14 | BAA01g13990 | A01 | 6664376 | C | T | downstream_gene_variant | MODIFIER | c.*2807C>T| |
S249 |
15 | BAA01g13990 | A01 | 6666528 | G | A | downstream_gene_variant | MODIFIER | c.*4959G>A| |
S96 |