Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05740 | A08 | 4417519 | C | T | missense_variant&splice_region_variant | MODERATE | c.1288G>A|p.Glu430Lys |
S47 |
2 | BAA08g05740 | A08 | 4418469 | C | T | missense_variant | MODERATE | c.712G>A|p.Glu238Lys |
S191 |
3 | BAA08g05740 | A08 | 4418717 | C | T | missense_variant | MODERATE | c.544G>A|p.Asp182Asn |
S281 |
4 | BAA08g05740 | A08 | 4419229 | C | T | missense_variant | MODERATE | c.181G>A|p.Glu61Lys |
S230 |
5 | BAA08g05740 | A08 | 4419419 | C | T | upstream_gene_variant | MODIFIER | c.-10G>A| |
S281 |
6 | BAA08g05740 | A08 | 4419955 | G | A | upstream_gene_variant | MODIFIER | c.-546C>T| |
S199 |
7 | BAA08g05740 | A08 | 4419964 | G | A | upstream_gene_variant | MODIFIER | c.-555C>T| |
S107 |
8 | BAA08g05740 | A08 | 4420454 | G | A | upstream_gene_variant | MODIFIER | c.-1045C>T| |
S40 S49 |
9 | BAA08g05740 | A08 | 4420832 | G | A | upstream_gene_variant | MODIFIER | c.-1423C>T| |
S257 |
10 | BAA08g05740 | A08 | 4421428 | C | T | upstream_gene_variant | MODIFIER | c.-2019G>A| |
S206 S26 |
11 | BAA08g05740 | A08 | 4421434 | C | T | upstream_gene_variant | MODIFIER | c.-2025G>A| |
S162 |
12 | BAA08g05740 | A08 | 4422838 | G | A | upstream_gene_variant | MODIFIER | c.-3429C>T| |
S16 |
13 | BAA08g05740 | A08 | 4424266 | G | A | upstream_gene_variant | MODIFIER | c.-4857C>T| |
S13 |
14 | BAA08g05740 | A08 | 4424389 | C | T | upstream_gene_variant | MODIFIER | c.-4980G>A| |
S162 |