Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27980 | A01 | 17064584 | C | T | upstream_gene_variant | MODIFIER | c.-4857C>T| |
S206 S26 |
2 | BAA01g27980 | A01 | 17067342 | C | T | upstream_gene_variant | MODIFIER | c.-2099C>T| |
S144 |
3 | BAA01g27980 | A01 | 17067517 | C | T | upstream_gene_variant | MODIFIER | c.-1924C>T| |
S148 |
4 | BAA01g27980 | A01 | 17067843 | C | T | upstream_gene_variant | MODIFIER | c.-1598C>T| |
S213 |
5 | BAA01g27980 | A01 | 17067929 | G | A | upstream_gene_variant | MODIFIER | c.-1512G>A| |
S278 |
6 | BAA01g27980 | A01 | 17068497 | G | A | upstream_gene_variant | MODIFIER | c.-944G>A| |
S202 |
7 | BAA01g27980 | A01 | 17068746 | G | A | upstream_gene_variant | MODIFIER | c.-695G>A| |
S262 |
8 | BAA01g27980 | A01 | 17069174 | C | T | upstream_gene_variant | MODIFIER | c.-267C>T| |
S277 |
9 | BAA01g27980 | A01 | 17069342 | C | T | upstream_gene_variant | MODIFIER | c.-99C>T| |
S120 |
10 | BAA01g27980 | A01 | 17069483 | G | A | missense_variant | MODERATE | c.43G>A|p.Glu15Lys |
S263 |
11 | BAA01g27980 | A01 | 17069870 | C | T | missense_variant | MODERATE | c.430C>T|p.Leu144Phe |
S185 S230 |
12 | BAA01g27980 | A01 | 17070397 | G | A | missense_variant | MODERATE | c.875G>A|p.Gly292Glu |
S302 |
13 | BAA01g27980 | A01 | 17071011 | G | A | missense_variant | MODERATE | c.1489G>A|p.Gly497Arg |
S238 |
14 | BAA01g27980 | A01 | 17071432 | G | A | missense_variant | MODERATE | c.1910G>A|p.Arg637Lys |
S119 |
15 | BAA01g27980 | A01 | 17072124 | C | T | downstream_gene_variant | MODIFIER | c.*259C>T| |
S11 |
16 | BAA01g27980 | A01 | 17072172 | G | A | downstream_gene_variant | MODIFIER | c.*307G>A| |
S152 |
17 | BAA01g27980 | A01 | 17072623 | C | T | downstream_gene_variant | MODIFIER | c.*758C>T| |
S117 S23 S266 S297 S55 S9 |
18 | BAA01g27980 | A01 | 17076015 | G | A | downstream_gene_variant | MODIFIER | c.*4150G>A| |
S302 |
19 | BAA01g27980 | A01 | 17076558 | C | T | downstream_gene_variant | MODIFIER | c.*4693C>T| |
S10 |