Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19070 | A10 | 17626959 | C | T | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S26 |
2 | BAA10g19070 | A10 | 17627138 | C | T | upstream_gene_variant | MODIFIER | c.-4766C>T| |
S249 |
3 | BAA10g19070 | A10 | 17627297 | G | A | upstream_gene_variant | MODIFIER | c.-4607G>A| |
S4 |
4 | BAA10g19070 | A10 | 17627772 | C | T | upstream_gene_variant | MODIFIER | c.-4132C>T| |
S246 |
5 | BAA10g19070 | A10 | 17628225 | C | T | upstream_gene_variant | MODIFIER | c.-3679C>T| |
S92 |
6 | BAA10g19070 | A10 | 17629523 | C | T | upstream_gene_variant | MODIFIER | c.-2381C>T| |
S195 |
7 | BAA10g19070 | A10 | 17629953 | C | T | upstream_gene_variant | MODIFIER | c.-1951C>T| |
S2 |
8 | BAA10g19070 | A10 | 17630678 | G | A | upstream_gene_variant | MODIFIER | c.-1226G>A| |
S212 |
9 | BAA10g19070 | A10 | 17630828 | G | A | upstream_gene_variant | MODIFIER | c.-1076G>A| |
S112 |
10 | BAA10g19070 | A10 | 17631616 | C | T | upstream_gene_variant | MODIFIER | c.-288C>T| |
S297 |
11 | BAA10g19070 | A10 | 17632538 | C | T | missense_variant | MODERATE | c.344C>T|p.Ser115Phe |
S130 |
12 | BAA10g19070 | A10 | 17632859 | C | T | synonymous_variant | LOW | c.564C>T|p.Asn188Asn |
S294 |
13 | BAA10g19070 | A10 | 17632889 | G | A | stop_gained | HIGH | c.594G>A|p.Trp198* |
S1 S90 |
14 | BAA10g19070 | A10 | 17633417 | C | T | downstream_gene_variant | MODIFIER | c.*370C>T| |
S238 |
15 | BAA10g19070 | A10 | 17634049 | G | A | downstream_gene_variant | MODIFIER | c.*1002G>A| |
S106 |
16 | BAA10g19070 | A10 | 17635226 | G | A | downstream_gene_variant | MODIFIER | c.*2179G>A| |
S25 |
17 | BAA10g19070 | A10 | 17635802 | G | A | downstream_gene_variant | MODIFIER | c.*2755G>A| |
S219 S72 |
18 | BAA10g19070 | A10 | 17637588 | G | A | downstream_gene_variant | MODIFIER | c.*4541G>A| |
S3 |