Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01890 | A08 | 1408766 | C | T | upstream_gene_variant | MODIFIER | c.-4596C>T| |
S236 |
2 | BAA08g01890 | A08 | 1409845 | C | T | upstream_gene_variant | MODIFIER | c.-3517C>T| |
S233 S291 |
3 | BAA08g01890 | A08 | 1410570 | G | A | upstream_gene_variant | MODIFIER | c.-2792G>A| |
S35 |
4 | BAA08g01890 | A08 | 1412487 | C | T | upstream_gene_variant | MODIFIER | c.-875C>T| |
S280 |
5 | BAA08g01890 | A08 | 1412952 | G | A | upstream_gene_variant | MODIFIER | c.-410G>A| |
S92 |
6 | BAA08g01890 | A08 | 1413054 | C | T | upstream_gene_variant | MODIFIER | c.-308C>T| |
S1 |
7 | BAA08g01890 | A08 | 1413383 | C | T | missense_variant | MODERATE | c.22C>T|p.Pro8Ser |
S305 |
8 | BAA08g01890 | A08 | 1413544 | C | T | synonymous_variant | LOW | c.183C>T|p.Ile61Ile |
S118 |
9 | BAA08g01890 | A08 | 1413873 | G | A | missense_variant | MODERATE | c.485G>A|p.Ser162Asn |
S182 |
10 | BAA08g01890 | A08 | 1415041 | G | A | downstream_gene_variant | MODIFIER | c.*1158G>A| |
S269 |
11 | BAA08g01890 | A08 | 1415702 | G | A | downstream_gene_variant | MODIFIER | c.*1819G>A| |
S301 S304 |
12 | BAA08g01890 | A08 | 1416134 | C | T | downstream_gene_variant | MODIFIER | c.*2251C>T| |
S170 |