Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01660 | A08 | 1204302 | C | T | missense_variant | MODERATE | c.1711G>A|p.Gly571Ser |
S231 |
2 | BAA08g01660 | A08 | 1204558 | G | A | synonymous_variant | LOW | c.1455C>T|p.Ile485Ile |
S263 |
3 | BAA08g01660 | A08 | 1206154 | C | T | splice_region_variant&intron_variant | LOW | c.580+8G>A| |
S4 |
4 | BAA08g01660 | A08 | 1207258 | G | A | upstream_gene_variant | MODIFIER | c.-177C>T| |
S297 |
5 | BAA08g01660 | A08 | 1210164 | G | A | upstream_gene_variant | MODIFIER | c.-3083C>T| |
S38 |
6 | BAA08g01660 | A08 | 1210594 | G | A | upstream_gene_variant | MODIFIER | c.-3513C>T| |
S39 |
7 | BAA08g01660 | A08 | 1211242 | C | T | upstream_gene_variant | MODIFIER | c.-4161G>A| |
S156 |
8 | BAA08g01660 | A08 | 1211259 | G | A | upstream_gene_variant | MODIFIER | c.-4178C>T| |
S206 |
9 | BAA08g01660 | A08 | 1211296 | C | T | upstream_gene_variant | MODIFIER | c.-4215G>A| |
S209 |
10 | BAA08g01660 | A08 | 1211946 | G | A | upstream_gene_variant | MODIFIER | c.-4865C>T| |
S72 |