Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10650 | A08 | 9555503 | G | A | synonymous_variant | LOW | c.2896C>T|p.Leu966Leu |
S287 |
2 | BAA08g10650 | A08 | 9555686 | C | T | missense_variant | MODERATE | c.2713G>A|p.Val905Ile |
S74 |
3 | BAA08g10650 | A08 | 9557199 | C | T | missense_variant&splice_region_variant | MODERATE | c.1771G>A|p.Glu591Lys |
S226 |
4 | BAA08g10650 | A08 | 9557357 | C | T | missense_variant | MODERATE | c.1613G>A|p.Gly538Asp |
S76 |
5 | BAA08g10650 | A08 | 9557418 | C | T | missense_variant | MODERATE | c.1552G>A|p.Val518Ile |
S284 |
6 | BAA08g10650 | A08 | 9557421 | C | T | missense_variant | MODERATE | c.1549G>A|p.Asp517Asn |
S215 |
7 | BAA08g10650 | A08 | 9559038 | C | T | stop_gained | HIGH | c.228G>A|p.Trp76* |
S60 |
8 | BAA08g10650 | A08 | 9559134 | C | T | synonymous_variant | LOW | c.132G>A|p.Arg44Arg |
S169 |
9 | BAA08g10650 | A08 | 9559551 | G | A | upstream_gene_variant | MODIFIER | c.-286C>T| |
S211 S227 |
10 | BAA08g10650 | A08 | 9560081 | G | A | upstream_gene_variant | MODIFIER | c.-816C>T| |
S90 |
11 | BAA08g10650 | A08 | 9560448 | G | A | upstream_gene_variant | MODIFIER | c.-1183C>T| |
S19 |
12 | BAA08g10650 | A08 | 9561759 | C | T | upstream_gene_variant | MODIFIER | c.-2494G>A| |
S80 |
13 | BAA08g10650 | A08 | 9562464 | C | T | upstream_gene_variant | MODIFIER | c.-3199G>A| |
S209 |
14 | BAA08g10650 | A08 | 9562659 | C | T | upstream_gene_variant | MODIFIER | c.-3394G>A| |
S172 S217 |
15 | BAA08g10650 | A08 | 9562843 | G | A | upstream_gene_variant | MODIFIER | c.-3578C>T| |
S133 |