Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22080 | A10 | 19163967 | C | T | upstream_gene_variant | MODIFIER | c.-4865C>T| |
S143 |
2 | BAA10g22080 | A10 | 19166569 | C | T | upstream_gene_variant | MODIFIER | c.-2263C>T| |
S229 |
3 | BAA10g22080 | A10 | 19166613 | C | T | upstream_gene_variant | MODIFIER | c.-2219C>T| |
S148 S210 S30 S31 |
4 | BAA10g22080 | A10 | 19167247 | G | A | upstream_gene_variant | MODIFIER | c.-1585G>A| |
S166 |
5 | BAA10g22080 | A10 | 19167502 | G | A | upstream_gene_variant | MODIFIER | c.-1330G>A| |
S117 |
6 | BAA10g22080 | A10 | 19167507 | G | A | upstream_gene_variant | MODIFIER | c.-1325G>A| |
S288 |
7 | BAA10g22080 | A10 | 19168136 | G | A | upstream_gene_variant | MODIFIER | c.-696G>A| |
S263 |
8 | BAA10g22080 | A10 | 19168318 | C | T | upstream_gene_variant | MODIFIER | c.-514C>T| |
S169 |
9 | BAA10g22080 | A10 | 19169764 | G | A | missense_variant | MODERATE | c.158G>A|p.Gly53Glu |
S273 |
10 | BAA10g22080 | A10 | 19170159 | C | T | intron_variant | MODIFIER | c.371-17C>T| |
S150 |
11 | BAA10g22080 | A10 | 19170358 | G | A | downstream_gene_variant | MODIFIER | c.*94G>A| |
S178 |
12 | BAA10g22080 | A10 | 19170371 | C | T | downstream_gene_variant | MODIFIER | c.*107C>T| |
S206 S26 |