Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21070 | A01 | 10371622 | G | A | downstream_gene_variant | MODIFIER | c.*1397C>T| |
S281 |
2 | BAA01g21070 | A01 | 10371716 | G | A | downstream_gene_variant | MODIFIER | c.*1303C>T| |
S294 |
3 | BAA01g21070 | A01 | 10373568 | C | T | intron_variant | MODIFIER | c.148-147G>A| |
S192 |
4 | BAA01g21070 | A01 | 10373656 | C | T | intron_variant | MODIFIER | c.147+166G>A| |
S272 |
5 | BAA01g21070 | A01 | 10373952 | C | T | missense_variant | MODERATE | c.40G>A|p.Asp14Asn |
S113 |
6 | BAA01g21070 | A01 | 10374120 | G | A | upstream_gene_variant | MODIFIER | c.-129C>T| |
S56 |
7 | BAA01g21070 | A01 | 10375160 | G | A | upstream_gene_variant | MODIFIER | c.-1169C>T| |
S143 |
8 | BAA01g21070 | A01 | 10375456 | G | A | upstream_gene_variant | MODIFIER | c.-1465C>T| |
S302 |
9 | BAA01g21070 | A01 | 10375726 | C | T | upstream_gene_variant | MODIFIER | c.-1735G>A| |
S228 |
10 | BAA01g21070 | A01 | 10376228 | C | T | upstream_gene_variant | MODIFIER | c.-2237G>A| |
S260 |
11 | BAA01g21070 | A01 | 10376477 | C | T | upstream_gene_variant | MODIFIER | c.-2486G>A| |
S4 |
12 | BAA01g21070 | A01 | 10376896 | T | A | upstream_gene_variant | MODIFIER | c.-2905A>T| |
S305 |
13 | BAA01g21070 | A01 | 10377162 | G | A | upstream_gene_variant | MODIFIER | c.-3171C>T| |
S32 |