| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 191951 | BAA02g26660 | A02 | 14914593 | G | A | upstream_gene_variant | MODIFIER | c.-3936G>A| |
S245 |
| 191952 | BAA02g26660 | A02 | 14915585 | C | T | upstream_gene_variant | MODIFIER | c.-2944C>T| |
S64 |
| 191953 | BAA02g26660 | A02 | 14915759 | C | T | upstream_gene_variant | MODIFIER | c.-2770C>T| |
S172 S217 |
| 191954 | BAA02g26660 | A02 | 14915858 | G | A | upstream_gene_variant | MODIFIER | c.-2671G>A| |
S288 |
| 191955 | BAA02g26660 | A02 | 14916209 | G | A | upstream_gene_variant | MODIFIER | c.-2320G>A| |
S269 |
| 191956 | BAA02g26660 | A02 | 14916949 | C | T | upstream_gene_variant | MODIFIER | c.-1580C>T| |
S97 |
| 191957 | BAA02g26660 | A02 | 14917307 | G | A | upstream_gene_variant | MODIFIER | c.-1222G>A| |
S47 |
| 191958 | BAA02g26660 | A02 | 14918433 | G | A | upstream_gene_variant | MODIFIER | c.-96G>A| |
S255 |
| 191959 | BAA02g26660 | A02 | 14918647 | C | T | intron_variant | MODIFIER | c.61+58C>T| |
S183 S198 |
| 191960 | BAA02g26660 | A02 | 14919489 | C | T | downstream_gene_variant | MODIFIER | c.*378C>T| |
S224 |
| 191961 | BAA02g26660 | A02 | 14921149 | C | T | downstream_gene_variant | MODIFIER | c.*2038C>T| |
S124 |
| 191962 | BAA02g26660 | A02 | 14921164 | C | T | downstream_gene_variant | MODIFIER | c.*2053C>T| |
S240 |
| 191963 | BAA02g26660 | A02 | 14921235 | G | A | downstream_gene_variant | MODIFIER | c.*2124G>A| |
S278 |
| 191964 | BAA02g26670 | A02 | 14923331 | C | T | upstream_gene_variant | MODIFIER | c.-2926C>T| |
S18 |
| 191965 | BAA02g26670 | A02 | 14923736 | G | A | upstream_gene_variant | MODIFIER | c.-2521G>A| |
S149 |
| 191966 | BAA02g26670 | A02 | 14924845 | G | A | upstream_gene_variant | MODIFIER | c.-1412G>A| |
S232 |
| 191967 | BAA02g26690 | A02 | 14934186 | C | T | upstream_gene_variant | MODIFIER | c.-980G>A| |
S296 |
| 191968 | BAA02g26690 | A02 | 14934217 | C | T | upstream_gene_variant | MODIFIER | c.-1011G>A| |
S233 |
| 191969 | BAA02g26700 | A02 | 14934553 | G | A | synonymous_variant | LOW | c.312G>A|p.Gln104Gln |
S59 |
| 191970 | BAA02g26700 | A02 | 14934557 | C | A | missense_variant | MODERATE | c.316C>A|p.Gln106Lys |
S138 |
| 191971 | BAA02g26690 | A02 | 14934731 | G | A | upstream_gene_variant | MODIFIER | c.-1525C>T| |
S223 |
| 191972 | BAA02g26690 | A02 | 14934800 | C | T | upstream_gene_variant | MODIFIER | c.-1594G>A| |
S255 |
| 191973 | BAA02g26690 | A02 | 14936385 | C | T | upstream_gene_variant | MODIFIER | c.-3179G>A| |
S177 |
| 191974 | BAA02g26710 | A02 | 14937870 | C | T | synonymous_variant | LOW | c.588C>T|p.Val196Val |
S167 |
| 191975 | BAA02g26710 | A02 | 14939780 | G | A | intron_variant | MODIFIER | c.907-977G>A| |
S122 S209 |