Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g04780 | A07 | 3975249 | C | T | upstream_gene_variant | MODIFIER | c.-4692C>T| |
S58 |
2 | BAA07g04780 | A07 | 3975255 | C | T | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S294 |
3 | BAA07g04780 | A07 | 3975277 | C | T | upstream_gene_variant | MODIFIER | c.-4664C>T| |
S142 |
4 | BAA07g04780 | A07 | 3976106 | G | A | upstream_gene_variant | MODIFIER | c.-3835G>A| |
S233 |
5 | BAA07g04780 | A07 | 3976393 | C | T | upstream_gene_variant | MODIFIER | c.-3548C>T| |
S81 |
6 | BAA07g04780 | A07 | 3977743 | G | A | upstream_gene_variant | MODIFIER | c.-2198G>A| |
S186 |
7 | BAA07g04780 | A07 | 3978170 | G | A | upstream_gene_variant | MODIFIER | c.-1771G>A| |
S206 S26 |
8 | BAA07g04780 | A07 | 3978287 | G | A | upstream_gene_variant | MODIFIER | c.-1654G>A| |
S28 |
9 | BAA07g04780 | A07 | 3980138 | G | A | synonymous_variant | LOW | c.198G>A|p.Pro66Pro |
S117 |
10 | BAA07g04780 | A07 | 3980605 | G | A | missense_variant&splice_region_variant | MODERATE | c.665G>A|p.Cys222Tyr |
S298 |
11 | BAA07g04780 | A07 | 3981931 | C | T | missense_variant | MODERATE | c.1036C>T|p.Pro346Ser |
S38 |
12 | BAA07g04780 | A07 | 3982103 | C | T | downstream_gene_variant | MODIFIER | c.*50C>T| |
|
13 | BAA07g04780 | A07 | 3984085 | G | A | downstream_gene_variant | MODIFIER | c.*2032G>A| |
S28 |