Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14120 | A02 | 6617575 | G | A | synonymous_variant | LOW | c.3174C>T|p.Asn1058Asn |
S228 |
2 | BAA02g14120 | A02 | 6620320 | C | T | missense_variant | MODERATE | c.1148G>A|p.Arg383Gln |
S212 |
3 | BAA02g14120 | A02 | 6622252 | G | A | intron_variant | MODIFIER | c.888-1575C>T| |
S265 |
4 | BAA02g14120 | A02 | 6622364 | A | T | intron_variant | MODIFIER | c.888-1687T>A| |
S228 |
5 | BAA02g14120 | A02 | 6623633 | G | A | intron_variant | MODIFIER | c.887+1243C>T| |
S225 |
6 | BAA02g14120 | A02 | 6626473 | G | A | upstream_gene_variant | MODIFIER | c.-20C>T| |
S113 S117 S23 S9 |
7 | BAA02g14120 | A02 | 6628012 | C | T | upstream_gene_variant | MODIFIER | c.-1559G>A| |
S252 |
8 | BAA02g14120 | A02 | 6628647 | C | T | upstream_gene_variant | MODIFIER | c.-2194G>A| |
S72 |
9 | BAA02g14120 | A02 | 6629763 | G | A | upstream_gene_variant | MODIFIER | c.-3310C>T| |
S291 |
10 | BAA02g14120 | A02 | 6631397 | G | A | upstream_gene_variant | MODIFIER | c.-4944C>T| |
S38 |