Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00570 | A10 | 282947 | G | A | upstream_gene_variant | MODIFIER | c.-2683G>A| |
S217 |
2 | BAA10g00570 | A10 | 282949 | G | A | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S33 |
3 | BAA10g00570 | A10 | 283361 | C | T | upstream_gene_variant | MODIFIER | c.-2269C>T| |
S294 |
4 | BAA10g00570 | A10 | 283980 | A | G | upstream_gene_variant | MODIFIER | c.-1650A>G| |
S167 |
5 | BAA10g00570 | A10 | 284038 | G | A | upstream_gene_variant | MODIFIER | c.-1592G>A| |
S20 |
6 | BAA10g00570 | A10 | 284157 | G | A | upstream_gene_variant | MODIFIER | c.-1473G>A| |
S157 S163 |
7 | BAA10g00570 | A10 | 284761 | T | A | upstream_gene_variant | MODIFIER | c.-869T>A| |
S259 |
8 | BAA10g00570 | A10 | 286102 | C | T | synonymous_variant | LOW | c.399C>T|p.Thr133Thr |
S237 |
9 | BAA10g00570 | A10 | 286261 | G | A | missense_variant | MODERATE | c.558G>A|p.Met186Ile |
S283 |
10 | BAA10g00570 | A10 | 286403 | G | A | missense_variant | MODERATE | c.700G>A|p.Asp234Asn |
S48 |
11 | BAA10g00570 | A10 | 286430 | C | T | missense_variant | MODERATE | c.727C>T|p.Pro243Ser |
S117 |
12 | BAA10g00570 | A10 | 290735 | G | A | downstream_gene_variant | MODIFIER | c.*4159G>A| |
S1 |
13 | BAA10g00570 | A10 | 291263 | G | A | downstream_gene_variant | MODIFIER | c.*4687G>A| |
S267 |