Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07890 | A10 | 4981545 | G | A | upstream_gene_variant | MODIFIER | c.-4711G>A| |
S148 S210 S30 S31 |
2 | BAA10g07890 | A10 | 4982444 | C | T | upstream_gene_variant | MODIFIER | c.-3812C>T| |
S114 |
3 | BAA10g07890 | A10 | 4983410 | G | A | upstream_gene_variant | MODIFIER | c.-2846G>A| |
S75 S81 |
4 | BAA10g07890 | A10 | 4985506 | C | T | upstream_gene_variant | MODIFIER | c.-750C>T| |
S294 |
5 | BAA10g07890 | A10 | 4986079 | C | T | upstream_gene_variant | MODIFIER | c.-177C>T| |
S242 |
6 | BAA10g07890 | A10 | 4986743 | G | A | intron_variant | MODIFIER | c.92-10G>A| |
S36 |
7 | BAA10g07890 | A10 | 4986982 | C | T | synonymous_variant | LOW | c.321C>T|p.Asn107Asn |
S238 |
8 | BAA10g07890 | A10 | 4987058 | C | T | intron_variant | MODIFIER | c.325+72C>T| |
S259 |
9 | BAA10g07890 | A10 | 4987529 | C | T | intron_variant | MODIFIER | c.419+279C>T| |
S136 S186 |
10 | BAA10g07890 | A10 | 4988025 | C | T | missense_variant | MODERATE | c.437C>T|p.Thr146Ile |
S8 |
11 | BAA10g07890 | A10 | 4988061 | C | T | missense_variant | MODERATE | c.473C>T|p.Pro158Leu |
S247 |
12 | BAA10g07890 | A10 | 4989179 | G | A | downstream_gene_variant | MODIFIER | c.*83G>A| |
S130 S160 |
13 | BAA10g07890 | A10 | 4989918 | G | A | downstream_gene_variant | MODIFIER | c.*822G>A| |
S202 |
14 | BAA10g07890 | A10 | 4990015 | G | A | downstream_gene_variant | MODIFIER | c.*919G>A| |
S202 |
15 | BAA10g07890 | A10 | 4990721 | G | A | downstream_gene_variant | MODIFIER | c.*1625G>A| |
S184 |
16 | BAA10g07890 | A10 | 4991259 | C | T | downstream_gene_variant | MODIFIER | c.*2163C>T| |
S10 |
17 | BAA10g07890 | A10 | 4991724 | C | T | downstream_gene_variant | MODIFIER | c.*2628C>T| |
S95 |