Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08180 | A10 | 5803070 | G | A | upstream_gene_variant | MODIFIER | c.-4091G>A| |
S164 |
2 | BAA10g08180 | A10 | 5804795 | G | A | upstream_gene_variant | MODIFIER | c.-2366G>A| |
S17 |
3 | BAA10g08180 | A10 | 5805019 | T | C | upstream_gene_variant | MODIFIER | c.-2142T>C| |
S292 |
4 | BAA10g08180 | A10 | 5805220 | G | A | upstream_gene_variant | MODIFIER | c.-1941G>A| |
S245 |
5 | BAA10g08180 | A10 | 5805401 | G | A | upstream_gene_variant | MODIFIER | c.-1760G>A| |
S53 |
6 | BAA10g08180 | A10 | 5805886 | G | A | upstream_gene_variant | MODIFIER | c.-1275G>A| |
S59 |
7 | BAA10g08180 | A10 | 5807089 | G | A | upstream_gene_variant | MODIFIER | c.-72G>A| |
S120 |
8 | BAA10g08180 | A10 | 5808309 | G | A | intron_variant | MODIFIER | c.836+232G>A| |
S148 S30 S31 |
9 | BAA10g08180 | A10 | 5809544 | C | T | intron_variant | MODIFIER | c.1433+20C>T| |
S10 |
10 | BAA10g08180 | A10 | 5809725 | C | T | intron_variant | MODIFIER | c.1434-9C>T| |
S259 |
11 | BAA10g08180 | A10 | 5810082 | C | T | intron_variant | MODIFIER | c.1719-16C>T| |
S152 S289 |
12 | BAA10g08180 | A10 | 5810713 | G | A | stop_gained | HIGH | c.2268G>A|p.Trp756* |
S69 |
13 | BAA10g08180 | A10 | 5811590 | C | T | intron_variant | MODIFIER | c.2937+28C>T| |
S200 |
14 | BAA10g08180 | A10 | 5811699 | G | A | missense_variant | MODERATE | c.2995G>A|p.Ala999Thr |
S295 |
15 | BAA10g08180 | A10 | 5812762 | G | A | missense_variant | MODERATE | c.3763G>A|p.Asp1255Asn |
S293 |
16 | BAA10g08180 | A10 | 5813014 | G | A | intron_variant | MODIFIER | c.3931-39G>A| |
S172 S217 |
17 | BAA10g08180 | A10 | 5813071 | C | T | missense_variant | MODERATE | c.3949C>T|p.Leu1317Phe |
S162 |
18 | BAA10g08180 | A10 | 5813664 | C | T | missense_variant | MODERATE | c.4346C>T|p.Pro1449Leu |
S256 |