Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39090 | A05 | 38245167 | C | T | upstream_gene_variant | MODIFIER | c.-4440C>T| |
S132 S215 |
2 | BAA05g39090 | A05 | 38245358 | C | T | upstream_gene_variant | MODIFIER | c.-4249C>T| |
S67 |
3 | BAA05g39090 | A05 | 38245542 | C | T | upstream_gene_variant | MODIFIER | c.-4065C>T| |
S167 |
4 | BAA05g39090 | A05 | 38246982 | C | T | upstream_gene_variant | MODIFIER | c.-2625C>T| |
S294 |
5 | BAA05g39090 | A05 | 38247107 | C | T | upstream_gene_variant | MODIFIER | c.-2500C>T| |
S237 |
6 | BAA05g39090 | A05 | 38247258 | A | T | upstream_gene_variant | MODIFIER | c.-2349A>T| |
S161 |
7 | BAA05g39090 | A05 | 38248352 | G | A | upstream_gene_variant | MODIFIER | c.-1255G>A| |
S5 |
8 | BAA05g39090 | A05 | 38248382 | G | A | upstream_gene_variant | MODIFIER | c.-1225G>A| |
S138 |
9 | BAA05g39090 | A05 | 38248720 | G | A | upstream_gene_variant | MODIFIER | c.-887G>A| |
S180 |
10 | BAA05g39090 | A05 | 38250370 | C | T | missense_variant | MODERATE | c.634C>T|p.Pro212Ser |
S1 S90 |
11 | BAA05g39090 | A05 | 38251608 | G | A | downstream_gene_variant | MODIFIER | c.*1052G>A| |
S119 |