Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03890 | A10 | 1899141 | C | T | downstream_gene_variant | MODIFIER | c.*3817G>A| |
S25 |
2 | BAA10g03890 | A10 | 1899464 | G | A | downstream_gene_variant | MODIFIER | c.*3494C>T| |
S257 |
3 | BAA10g03890 | A10 | 1899485 | C | T | downstream_gene_variant | MODIFIER | c.*3473G>A| |
S177 |
4 | BAA10g03890 | A10 | 1900720 | C | T | downstream_gene_variant | MODIFIER | c.*2238G>A| |
S42 |
5 | BAA10g03890 | A10 | 1900972 | G | A | downstream_gene_variant | MODIFIER | c.*1986C>T| |
S278 |
6 | BAA10g03890 | A10 | 1901171 | G | A | downstream_gene_variant | MODIFIER | c.*1787C>T| |
S242 |
7 | BAA10g03890 | A10 | 1901663 | G | A | downstream_gene_variant | MODIFIER | c.*1295C>T| |
S13 |
8 | BAA10g03890 | A10 | 1901832 | C | T | downstream_gene_variant | MODIFIER | c.*1126G>A| |
S143 |
9 | BAA10g03890 | A10 | 1902257 | G | A | downstream_gene_variant | MODIFIER | c.*701C>T| |
S120 |
10 | BAA10g03890 | A10 | 1902456 | G | A | downstream_gene_variant | MODIFIER | c.*502C>T| |
S16 |
11 | BAA10g03890 | A10 | 1903130 | C | T | intron_variant | MODIFIER | c.70-35G>A| |
S104 S52 |
12 | BAA10g03890 | A10 | 1904147 | G | A | intron_variant | MODIFIER | c.69+44C>T| |
S156 |
13 | BAA10g03890 | A10 | 1904724 | C | T | upstream_gene_variant | MODIFIER | c.-465G>A| |
S247 |
14 | BAA10g03890 | A10 | 1905037 | G | A | upstream_gene_variant | MODIFIER | c.-778C>T| |
S219 S72 |
15 | BAA10g03890 | A10 | 1905139 | G | A | upstream_gene_variant | MODIFIER | c.-880C>T| |
S156 |
16 | BAA10g03890 | A10 | 1905534 | G | A | upstream_gene_variant | MODIFIER | c.-1275C>T| |
S33 |
17 | BAA10g03890 | A10 | 1905905 | C | T | upstream_gene_variant | MODIFIER | c.-1646G>A| |
S146 |
18 | BAA10g03890 | A10 | 1906372 | C | T | upstream_gene_variant | MODIFIER | c.-2113G>A| |
S276 |