Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g17070 | A07 | 23548413 | C | T | missense_variant | MODERATE | c.3194G>A|p.Arg1065His |
S297 |
2 | BAA07g17070 | A07 | 23549531 | C | T | missense_variant | MODERATE | c.2276G>A|p.Ser759Asn |
S130 |
3 | BAA07g17070 | A07 | 23549546 | G | A | missense_variant | MODERATE | c.2261C>T|p.Ala754Val |
S65 |
4 | BAA07g17070 | A07 | 23549637 | C | T | missense_variant | MODERATE | c.2170G>A|p.Val724Ile |
S155 S211 |
5 | BAA07g17070 | A07 | 23549735 | C | T | missense_variant | MODERATE | c.2072G>A|p.Gly691Asp |
S32 |
6 | BAA07g17070 | A07 | 23550051 | G | A | missense_variant | MODERATE | c.1756C>T|p.Pro586Ser |
S244 |
7 | BAA07g17070 | A07 | 23550663 | G | A | stop_gained | HIGH | c.1225C>T|p.Gln409* |
S244 |
8 | BAA07g17070 | A07 | 23551057 | G | A | missense_variant | MODERATE | c.950C>T|p.Thr317Ile |
S190 |
9 | BAA07g17070 | A07 | 23551081 | G | A | missense_variant | MODERATE | c.926C>T|p.Ser309Phe |
S138 |
10 | BAA07g17070 | A07 | 23551249 | G | A | synonymous_variant | LOW | c.855C>T|p.Ile285Ile |
S278 |
11 | BAA07g17070 | A07 | 23551277 | C | T | missense_variant | MODERATE | c.827G>A|p.Arg276Gln |
S262 |
12 | BAA07g17070 | A07 | 23553123 | G | A | upstream_gene_variant | MODIFIER | c.-416C>T| |
S40 S49 |
13 | BAA07g17070 | A07 | 23553474 | C | T | upstream_gene_variant | MODIFIER | c.-767G>A| |
S85 |
14 | BAA07g17070 | A07 | 23554578 | C | T | upstream_gene_variant | MODIFIER | c.-1871G>A| |
S275 |
15 | BAA07g17070 | A07 | 23554684 | C | T | upstream_gene_variant | MODIFIER | c.-1977G>A| |
S41 |
16 | BAA07g17070 | A07 | 23554721 | G | A | upstream_gene_variant | MODIFIER | c.-2014C>T| |
S244 |
17 | BAA07g17070 | A07 | 23556638 | G | A | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S87 |
18 | BAA07g17070 | A07 | 23557513 | C | T | upstream_gene_variant | MODIFIER | c.-4806G>A| |
S19 |