Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01650 | A08 | 1196004 | G | A | upstream_gene_variant | MODIFIER | c.-3583G>A| |
S72 |
2 | BAA08g01650 | A08 | 1196789 | C | T | upstream_gene_variant | MODIFIER | c.-2798C>T| |
S171 |
3 | BAA08g01650 | A08 | 1197127 | G | A | upstream_gene_variant | MODIFIER | c.-2460G>A| |
S180 |
4 | BAA08g01650 | A08 | 1198063 | C | T | upstream_gene_variant | MODIFIER | c.-1524C>T| |
S295 |
5 | BAA08g01650 | A08 | 1198826 | G | A | upstream_gene_variant | MODIFIER | c.-761G>A| |
S19 |
6 | BAA08g01650 | A08 | 1199518 | C | T | upstream_gene_variant | MODIFIER | c.-69C>T| |
S67 |
7 | BAA08g01650 | A08 | 1199746 | G | A | missense_variant | MODERATE | c.160G>A|p.Asp54Asn |
S18 |
8 | BAA08g01650 | A08 | 1200100 | C | T | missense_variant | MODERATE | c.514C>T|p.Pro172Ser |
S47 |
9 | BAA08g01650 | A08 | 1202905 | C | T | downstream_gene_variant | MODIFIER | c.*2293C>T| |
S7 |
10 | BAA08g01650 | A08 | 1204045 | C | T | downstream_gene_variant | MODIFIER | c.*3433C>T| |
S105 S106 |