Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g43680 | A07 | 37321006 | C | T | upstream_gene_variant | MODIFIER | c.-4256C>T| |
S122 |
2 | BAA07g43680 | A07 | 37321722 | G | A | upstream_gene_variant | MODIFIER | c.-3540G>A| |
S292 |
3 | BAA07g43680 | A07 | 37322644 | C | T | upstream_gene_variant | MODIFIER | c.-2618C>T| |
S116 |
4 | BAA07g43680 | A07 | 37322817 | G | A | upstream_gene_variant | MODIFIER | c.-2445G>A| |
S57 |
5 | BAA07g43680 | A07 | 37322944 | C | T | upstream_gene_variant | MODIFIER | c.-2318C>T| |
S94 |
6 | BAA07g43680 | A07 | 37323427 | G | A | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S70 |
7 | BAA07g43680 | A07 | 37323539 | C | T | upstream_gene_variant | MODIFIER | c.-1723C>T| |
S295 |
8 | BAA07g43680 | A07 | 37323669 | C | T | upstream_gene_variant | MODIFIER | c.-1593C>T| |
S67 |
9 | BAA07g43680 | A07 | 37323686 | G | A | upstream_gene_variant | MODIFIER | c.-1576G>A| |
S178 |
10 | BAA07g43680 | A07 | 37324499 | G | A | upstream_gene_variant | MODIFIER | c.-763G>A| |
S76 |
11 | BAA07g43680 | A07 | 37325040 | G | A | upstream_gene_variant | MODIFIER | c.-222G>A| |
S216 |
12 | BAA07g43680 | A07 | 37325673 | C | T | missense_variant | MODERATE | c.335C>T|p.Thr112Ile |
S157 S167 S257 S262 |
13 | BAA07g43680 | A07 | 37326027 | G | A | missense_variant | MODERATE | c.514G>A|p.Gly172Arg |
S231 |