Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09310 | A10 | 11305713 | C | T | upstream_gene_variant | MODIFIER | c.-1540C>T| |
S149 |
2 | BAA10g09310 | A10 | 11305716 | C | T | upstream_gene_variant | MODIFIER | c.-1537C>T| |
S249 |
3 | BAA10g09310 | A10 | 11306598 | G | A | upstream_gene_variant | MODIFIER | c.-655G>A| |
S237 |
4 | BAA10g09310 | A10 | 11306743 | C | T | upstream_gene_variant | MODIFIER | c.-510C>T| |
S4 |
5 | BAA10g09310 | A10 | 11307626 | C | T | missense_variant | MODERATE | c.374C>T|p.Thr125Met |
S40 S49 |
6 | BAA10g09310 | A10 | 11308063 | C | T | stop_gained | HIGH | c.811C>T|p.Gln271* |
S173 |
7 | BAA10g09310 | A10 | 11308697 | G | A | missense_variant | MODERATE | c.1192G>A|p.Asp398Asn |
S68 |
8 | BAA10g09310 | A10 | 11310325 | C | T | synonymous_variant | LOW | c.2019C>T|p.Ile673Ile |
S287 |
9 | BAA10g09310 | A10 | 11310419 | C | T | missense_variant | MODERATE | c.2113C>T|p.His705Tyr |
S5 |
10 | BAA10g09310 | A10 | 11310602 | C | T | synonymous_variant | LOW | c.2296C>T|p.Leu766Leu |
S181 |
11 | BAA10g09310 | A10 | 11310626 | C | T | missense_variant | MODERATE | c.2320C>T|p.Leu774Phe |
S162 |
12 | BAA10g09310 | A10 | 11310648 | C | T | missense_variant | MODERATE | c.2342C>T|p.Ala781Val |
S196 |
13 | BAA10g09310 | A10 | 11310954 | G | A | downstream_gene_variant | MODIFIER | c.*182G>A| |
S150 |