Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09400 | A10 | 11397188 | G | A | upstream_gene_variant | MODIFIER | c.-4694G>A| |
S139 |
2 | BAA10g09400 | A10 | 11397202 | C | T | upstream_gene_variant | MODIFIER | c.-4680C>T| |
S103 |
3 | BAA10g09400 | A10 | 11397335 | C | T | upstream_gene_variant | MODIFIER | c.-4547C>T| |
S177 |
4 | BAA10g09400 | A10 | 11397563 | G | A | upstream_gene_variant | MODIFIER | c.-4319G>A| |
S157 S163 |
5 | BAA10g09400 | A10 | 11398363 | C | T | upstream_gene_variant | MODIFIER | c.-3519C>T| |
S124 |
6 | BAA10g09400 | A10 | 11398522 | C | T | upstream_gene_variant | MODIFIER | c.-3360C>T| |
S244 |
7 | BAA10g09400 | A10 | 11399068 | C | T | upstream_gene_variant | MODIFIER | c.-2814C>T| |
S203 |
8 | BAA10g09400 | A10 | 11399592 | C | A | upstream_gene_variant | MODIFIER | c.-2290C>A| |
S36 |
9 | BAA10g09400 | A10 | 11400460 | C | T | upstream_gene_variant | MODIFIER | c.-1422C>T| |
S256 |
10 | BAA10g09400 | A10 | 11400711 | C | T | upstream_gene_variant | MODIFIER | c.-1171C>T| |
S12 |
11 | BAA10g09400 | A10 | 11401108 | C | T | upstream_gene_variant | MODIFIER | c.-774C>T| |
S287 |
12 | BAA10g09400 | A10 | 11401490 | G | A | upstream_gene_variant | MODIFIER | c.-392G>A| |
S217 |
13 | BAA10g09400 | A10 | 11401659 | G | A | upstream_gene_variant | MODIFIER | c.-223G>A| |
S36 |
14 | BAA10g09400 | A10 | 11402488 | G | A | missense_variant | MODERATE | c.607G>A|p.Gly203Ser |
S237 |
15 | BAA10g09400 | A10 | 11402533 | G | A | missense_variant | MODERATE | c.652G>A|p.Glu218Lys |
S226 |
16 | BAA10g09400 | A10 | 11404822 | C | T | downstream_gene_variant | MODIFIER | c.*1090C>T| |
S193 |
17 | BAA10g09400 | A10 | 11406035 | C | T | downstream_gene_variant | MODIFIER | c.*2303C>T| |
S206 S26 |