Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g06690 | A05 | 3254084 | G | A | missense_variant | MODERATE | c.1040C>T|p.Thr347Met |
S111 |
2 | BAA05g06690 | A05 | 3256221 | G | A | upstream_gene_variant | MODIFIER | c.-249C>T| |
S296 |
3 | BAA05g06690 | A05 | 3256349 | G | A | upstream_gene_variant | MODIFIER | c.-377C>T| |
S218 |
4 | BAA05g06690 | A05 | 3256600 | G | A | upstream_gene_variant | MODIFIER | c.-628C>T| |
S32 |
5 | BAA05g06690 | A05 | 3257524 | G | A | upstream_gene_variant | MODIFIER | c.-1552C>T| |
S244 |
6 | BAA05g06690 | A05 | 3258775 | G | A | upstream_gene_variant | MODIFIER | c.-2803C>T| |
S224 |
7 | BAA05g06690 | A05 | 3259078 | G | A | upstream_gene_variant | MODIFIER | c.-3106C>T| |
S15 S3 |
8 | BAA05g06690 | A05 | 3260159 | C | T | upstream_gene_variant | MODIFIER | c.-4187G>A| |
S205 |
9 | BAA05g06690 | A05 | 3260262 | C | T | upstream_gene_variant | MODIFIER | c.-4290G>A| |
S12 |
10 | BAA05g06690 | A05 | 3260263 | C | T | upstream_gene_variant | MODIFIER | c.-4291G>A| |
S20 |
11 | BAA05g06690 | A05 | 3260278 | C | T | upstream_gene_variant | MODIFIER | c.-4306G>A| |
S13 S140 S168 S279 |
12 | BAA05g06690 | A05 | 3260342 | C | T | upstream_gene_variant | MODIFIER | c.-4370G>A| |
S206 S26 |
13 | BAA05g06690 | A05 | 3260372 | G | A | upstream_gene_variant | MODIFIER | c.-4400C>T| |
S79 S91 |