Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10950 | A10 | 12697645 | C | T | downstream_gene_variant | MODIFIER | c.*4301G>A| |
S256 |
2 | BAA10g10950 | A10 | 12698277 | G | A | downstream_gene_variant | MODIFIER | c.*3669C>T| |
S13 |
3 | BAA10g10950 | A10 | 12698732 | G | A | downstream_gene_variant | MODIFIER | c.*3214C>T| |
S293 |
4 | BAA10g10950 | A10 | 12698978 | C | T | downstream_gene_variant | MODIFIER | c.*2968G>A| |
S81 S85 |
5 | BAA10g10950 | A10 | 12699281 | C | T | downstream_gene_variant | MODIFIER | c.*2665G>A| |
S149 |
6 | BAA10g10950 | A10 | 12699446 | C | T | downstream_gene_variant | MODIFIER | c.*2500G>A| |
S277 |
7 | BAA10g10950 | A10 | 12699895 | G | A | downstream_gene_variant | MODIFIER | c.*2051C>T| |
S151 S263 |
8 | BAA10g10950 | A10 | 12701725 | G | A | downstream_gene_variant | MODIFIER | c.*221C>T| |
S250 |
9 | BAA10g10950 | A10 | 12702112 | G | A | missense_variant | MODERATE | c.686C>T|p.Ser229Phe |
S158 |
10 | BAA10g10950 | A10 | 12702879 | C | T | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S224 |
11 | BAA10g10950 | A10 | 12703104 | C | T | upstream_gene_variant | MODIFIER | c.-222G>A| |
S40 S49 |
12 | BAA10g10950 | A10 | 12703867 | C | T | upstream_gene_variant | MODIFIER | c.-985G>A| |
S173 |
13 | BAA10g10950 | A10 | 12704002 | C | T | upstream_gene_variant | MODIFIER | c.-1120G>A| |
S204 |
14 | BAA10g10950 | A10 | 12704626 | G | A | upstream_gene_variant | MODIFIER | c.-1744C>T| |
S207 |
15 | BAA10g10950 | A10 | 12706924 | G | A | upstream_gene_variant | MODIFIER | c.-4042C>T| |
S289 |
16 | BAA10g10950 | A10 | 12707042 | G | A | upstream_gene_variant | MODIFIER | c.-4160C>T| |
S158 |
17 | BAA10g10950 | A10 | 12707350 | C | T | upstream_gene_variant | MODIFIER | c.-4468G>A| |
S146 |