Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27930 | A01 | 17004171 | C | T | upstream_gene_variant | MODIFIER | c.-4592C>T| |
S107 |
2 | BAA01g27930 | A01 | 17006497 | C | T | upstream_gene_variant | MODIFIER | c.-2266C>T| |
S69 |
3 | BAA01g27930 | A01 | 17007005 | C | T | upstream_gene_variant | MODIFIER | c.-1758C>T| |
S87 |
4 | BAA01g27930 | A01 | 17007260 | C | T | upstream_gene_variant | MODIFIER | c.-1503C>T| |
S112 |
5 | BAA01g27930 | A01 | 17007553 | G | A | upstream_gene_variant | MODIFIER | c.-1210G>A| |
S174 S216 |
6 | BAA01g27930 | A01 | 17007689 | C | T | upstream_gene_variant | MODIFIER | c.-1074C>T| |
S210 |
7 | BAA01g27930 | A01 | 17008720 | A | C | upstream_gene_variant | MODIFIER | c.-43A>C| |
S134 |
8 | BAA01g27930 | A01 | 17008800 | G | A | missense_variant | MODERATE | c.38G>A|p.Gly13Glu |
S2 |
9 | BAA01g27930 | A01 | 17010261 | C | T | intron_variant | MODIFIER | c.194-914C>T| |
S98 |
10 | BAA01g27930 | A01 | 17011393 | C | T | missense_variant | MODERATE | c.412C>T|p.His138Tyr |
S242 |
11 | BAA01g27930 | A01 | 17011445 | G | A | missense_variant | MODERATE | c.464G>A|p.Arg155Gln |
S62 |
12 | BAA01g27930 | A01 | 17012028 | G | A | synonymous_variant | LOW | c.972G>A|p.Lys324Lys |
S262 |
13 | BAA01g27930 | A01 | 17013311 | G | A | missense_variant | MODERATE | c.1876G>A|p.Asp626Asn |
S86 |
14 | BAA01g27930 | A01 | 17014339 | C | T | downstream_gene_variant | MODIFIER | c.*330C>T| |
S223 |