Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g07980 | A08 | 7265640 | C | T | upstream_gene_variant | MODIFIER | c.-4773C>T| |
S59 |
2 | BAA08g07980 | A08 | 7266215 | C | T | upstream_gene_variant | MODIFIER | c.-4198C>T| |
S167 |
3 | BAA08g07980 | A08 | 7266363 | G | A | upstream_gene_variant | MODIFIER | c.-4050G>A| |
S286 |
4 | BAA08g07980 | A08 | 7267014 | C | T | upstream_gene_variant | MODIFIER | c.-3399C>T| |
S71 |
5 | BAA08g07980 | A08 | 7267397 | G | A | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S19 |
6 | BAA08g07980 | A08 | 7268267 | C | T | upstream_gene_variant | MODIFIER | c.-2146C>T| |
S144 |
7 | BAA08g07980 | A08 | 7268477 | C | T | upstream_gene_variant | MODIFIER | c.-1936C>T| |
S44 |
8 | BAA08g07980 | A08 | 7268625 | G | A | upstream_gene_variant | MODIFIER | c.-1788G>A| |
S136 |
9 | BAA08g07980 | A08 | 7270568 | C | T | synonymous_variant | LOW | c.156C>T|p.Thr52Thr |
S32 |
10 | BAA08g07980 | A08 | 7270632 | G | A | missense_variant | MODERATE | c.220G>A|p.Asp74Asn |
S190 |
11 | BAA08g07980 | A08 | 7271094 | G | A | intron_variant | MODIFIER | c.631+51G>A| |
S16 |
12 | BAA08g07980 | A08 | 7271572 | G | A | missense_variant | MODERATE | c.925G>A|p.Val309Met |
S264 |
13 | BAA08g07980 | A08 | 7272148 | C | T | downstream_gene_variant | MODIFIER | c.*61C>T| |
S177 |