Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05790 | A10 | 2971220 | C | T | downstream_gene_variant | MODIFIER | c.*2096G>A| |
S87 |
2 | BAA10g05790 | A10 | 2971438 | C | T | downstream_gene_variant | MODIFIER | c.*1878G>A| |
S196 |
3 | BAA10g05790 | A10 | 2971536 | C | T | downstream_gene_variant | MODIFIER | c.*1780G>A| |
S132 S137 S215 S237 S89 |
4 | BAA10g05790 | A10 | 2972359 | C | T | downstream_gene_variant | MODIFIER | c.*957G>A| |
S73 S91 |
5 | BAA10g05790 | A10 | 2972403 | G | A | downstream_gene_variant | MODIFIER | c.*913C>T| |
S198 |
6 | BAA10g05790 | A10 | 2972688 | G | A | downstream_gene_variant | MODIFIER | c.*628C>T| |
S278 |
7 | BAA10g05790 | A10 | 2972906 | G | A | downstream_gene_variant | MODIFIER | c.*410C>T| |
S18 |
8 | BAA10g05790 | A10 | 2973408 | G | A | stop_gained | HIGH | c.94C>T|p.Arg32* |
S45 |
9 | BAA10g05790 | A10 | 2973449 | C | T | missense_variant | MODERATE | c.53G>A|p.Arg18His |
S195 |
10 | BAA10g05790 | A10 | 2974645 | G | A | upstream_gene_variant | MODIFIER | c.-1144C>T| |
S280 |
11 | BAA10g05790 | A10 | 2975213 | G | A | upstream_gene_variant | MODIFIER | c.-1712C>T| |
S241 |
12 | BAA10g05790 | A10 | 2975554 | G | A | upstream_gene_variant | MODIFIER | c.-2053C>T| |
S33 |
13 | BAA10g05790 | A10 | 2975645 | G | A | upstream_gene_variant | MODIFIER | c.-2144C>T| |
S218 |
14 | BAA10g05790 | A10 | 2977941 | C | T | upstream_gene_variant | MODIFIER | c.-4440G>A| |
S162 |