Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12960 | A10 | 14228024 | C | T | upstream_gene_variant | MODIFIER | c.-3379C>T| |
S108 |
2 | BAA10g12960 | A10 | 14228124 | G | A | upstream_gene_variant | MODIFIER | c.-3279G>A| |
S155 S211 |
3 | BAA10g12960 | A10 | 14228311 | C | T | upstream_gene_variant | MODIFIER | c.-3092C>T| |
S98 |
4 | BAA10g12960 | A10 | 14229785 | G | A | upstream_gene_variant | MODIFIER | c.-1618G>A| |
S195 |
5 | BAA10g12960 | A10 | 14232026 | G | A | missense_variant | MODERATE | c.529G>A|p.Asp177Asn |
S128 |
6 | BAA10g12960 | A10 | 14232174 | G | A | missense_variant | MODERATE | c.677G>A|p.Gly226Asp |
S219 S72 |
7 | BAA10g12960 | A10 | 14232465 | C | T | missense_variant | MODERATE | c.968C>T|p.Thr323Met |
S61 |
8 | BAA10g12960 | A10 | 14232680 | G | A | missense_variant | MODERATE | c.1183G>A|p.Gly395Ser |
S15 |
9 | BAA10g12960 | A10 | 14233765 | C | T | downstream_gene_variant | MODIFIER | c.*582C>T| |
S38 |
10 | BAA10g12960 | A10 | 14234600 | C | T | downstream_gene_variant | MODIFIER | c.*1417C>T| |
S162 |
11 | BAA10g12960 | A10 | 14234744 | G | A | downstream_gene_variant | MODIFIER | c.*1561G>A| |
S212 |