Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g23890 | A07 | 27484794 | C | T | upstream_gene_variant | MODIFIER | c.-3263C>T| |
S244 |
2 | BAA07g23890 | A07 | 27485852 | G | A | upstream_gene_variant | MODIFIER | c.-2205G>A| |
S110 |
3 | BAA07g23890 | A07 | 27486033 | C | T | upstream_gene_variant | MODIFIER | c.-2024C>T| |
S281 |
4 | BAA07g23890 | A07 | 27486176 | G | A | upstream_gene_variant | MODIFIER | c.-1881G>A| |
S178 |
5 | BAA07g23890 | A07 | 27486451 | C | T | upstream_gene_variant | MODIFIER | c.-1606C>T| |
S148 |
6 | BAA07g23890 | A07 | 27487329 | T | G | upstream_gene_variant | MODIFIER | c.-728T>G| |
S10 S154 S241 S302 S45 S61 |
7 | BAA07g23890 | A07 | 27487524 | C | T | upstream_gene_variant | MODIFIER | c.-533C>T| |
S274 |
8 | BAA07g23890 | A07 | 27487631 | C | T | upstream_gene_variant | MODIFIER | c.-426C>T| |
S148 S210 |
9 | BAA07g23890 | A07 | 27488317 | G | A | synonymous_variant | LOW | c.261G>A|p.Lys87Lys |
S84 S93 |
10 | BAA07g23890 | A07 | 27489575 | C | T | downstream_gene_variant | MODIFIER | c.*491C>T| |
S231 S302 |
11 | BAA07g23890 | A07 | 27489618 | T | A | downstream_gene_variant | MODIFIER | c.*534T>A| |
S3 |
12 | BAA07g23890 | A07 | 27489673 | G | A | downstream_gene_variant | MODIFIER | c.*589G>A| |
S234 |
13 | BAA07g23890 | A07 | 27489742 | G | A | downstream_gene_variant | MODIFIER | c.*658G>A| |
S183 S198 |
14 | BAA07g23890 | A07 | 27490027 | C | T | downstream_gene_variant | MODIFIER | c.*943C>T| |
S217 |
15 | BAA07g23890 | A07 | 27490259 | C | T | downstream_gene_variant | MODIFIER | c.*1175C>T| |
S37 |
16 | BAA07g23890 | A07 | 27490675 | C | T | downstream_gene_variant | MODIFIER | c.*1591C>T| |
S230 |
17 | BAA07g23890 | A07 | 27492477 | C | T | downstream_gene_variant | MODIFIER | c.*3393C>T| |
S94 |
18 | BAA07g23890 | A07 | 27493305 | C | T | downstream_gene_variant | MODIFIER | c.*4221C>T| |
S3 |
19 | BAA07g23890 | A07 | 27493504 | G | A | downstream_gene_variant | MODIFIER | c.*4420G>A| |
S182 S185 |