Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11900 | A10 | 13455038 | C | T | upstream_gene_variant | MODIFIER | c.-3622C>T| |
S87 |
2 | BAA10g11900 | A10 | 13455882 | G | A | upstream_gene_variant | MODIFIER | c.-2778G>A| |
S264 |
3 | BAA10g11900 | A10 | 13457516 | G | A | upstream_gene_variant | MODIFIER | c.-1144G>A| |
S279 |
4 | BAA10g11900 | A10 | 13457696 | C | T | upstream_gene_variant | MODIFIER | c.-964C>T| |
S298 |
5 | BAA10g11900 | A10 | 13458396 | G | A | upstream_gene_variant | MODIFIER | c.-264G>A| |
S274 |
6 | BAA10g11900 | A10 | 13459462 | C | T | missense_variant | MODERATE | c.803C>T|p.Ser268Phe |
S44 |
7 | BAA10g11900 | A10 | 13460549 | G | A | missense_variant | MODERATE | c.1890G>A|p.Met630Ile |
S296 |
8 | BAA10g11900 | A10 | 13461119 | G | A | stop_gained | HIGH | c.2460G>A|p.Trp820* |
S148 S210 S30 S31 |
9 | BAA10g11900 | A10 | 13461125 | G | A | synonymous_variant | LOW | c.2466G>A|p.Val822Val |
S207 |
10 | BAA10g11900 | A10 | 13461341 | G | A | synonymous_variant | LOW | c.2682G>A|p.Pro894Pro |
S48 |
11 | BAA10g11900 | A10 | 13463077 | C | T | downstream_gene_variant | MODIFIER | c.*1415C>T| |
S180 |
12 | BAA10g11900 | A10 | 13463305 | C | T | downstream_gene_variant | MODIFIER | c.*1643C>T| |
S68 |
13 | BAA10g11900 | A10 | 13464097 | C | T | downstream_gene_variant | MODIFIER | c.*2435C>T| |
S96 |
14 | BAA10g11900 | A10 | 13464794 | C | A | downstream_gene_variant | MODIFIER | c.*3132C>A| |
S13 S140 S219 S279 S64 S72 |
15 | BAA10g11900 | A10 | 13465700 | G | A | downstream_gene_variant | MODIFIER | c.*4038G>A| |
S66 |
16 | BAA10g11900 | A10 | 13465926 | C | T | downstream_gene_variant | MODIFIER | c.*4264C>T| |
S242 |
17 | BAA10g11900 | A10 | 13465962 | C | T | downstream_gene_variant | MODIFIER | c.*4300C>T| |
S294 |