Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04170 | A10 | 2082232 | C | T | missense_variant | MODERATE | c.22G>A|p.Gly8Ser |
S246 |
2 | BAA10g04170 | A10 | 2082476 | G | A | upstream_gene_variant | MODIFIER | c.-223C>T| |
S264 |
3 | BAA10g04170 | A10 | 2082973 | G | A | upstream_gene_variant | MODIFIER | c.-720C>T| |
S171 |
4 | BAA10g04170 | A10 | 2083011 | G | A | upstream_gene_variant | MODIFIER | c.-758C>T| |
S236 |
5 | BAA10g04170 | A10 | 2083480 | G | A | upstream_gene_variant | MODIFIER | c.-1227C>T| |
S301 S304 |
6 | BAA10g04170 | A10 | 2084001 | C | T | upstream_gene_variant | MODIFIER | c.-1748G>A| |
S87 |
7 | BAA10g04170 | A10 | 2084607 | C | T | upstream_gene_variant | MODIFIER | c.-2354G>A| |
S155 S211 |
8 | BAA10g04170 | A10 | 2084901 | C | T | upstream_gene_variant | MODIFIER | c.-2648G>A| |
S84 S93 |
9 | BAA10g04170 | A10 | 2084906 | C | T | upstream_gene_variant | MODIFIER | c.-2653G>A| |
S155 S211 |
10 | BAA10g04170 | A10 | 2085055 | C | T | upstream_gene_variant | MODIFIER | c.-2802G>A| |
S286 |
11 | BAA10g04170 | A10 | 2085577 | C | T | upstream_gene_variant | MODIFIER | c.-3324G>A| |
S61 |
12 | BAA10g04170 | A10 | 2086688 | C | T | upstream_gene_variant | MODIFIER | c.-4435G>A| |
S124 |
13 | BAA10g04170 | A10 | 2087186 | G | A | upstream_gene_variant | MODIFIER | c.-4933C>T| |
S295 |