| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 163951 | BAA02g10570 | A02 | 4706564 | C | T | upstream_gene_variant | MODIFIER | c.-3881G>A| |
S108 |
| 163952 | BAA02g10570 | A02 | 4706827 | G | A | upstream_gene_variant | MODIFIER | c.-4144C>T| |
S37 |
| 163953 | BAA02g10590 | A02 | 4707743 | C | T | upstream_gene_variant | MODIFIER | c.-2166C>T| |
S178 |
| 163954 | BAA02g10590 | A02 | 4710179 | G | A | missense_variant | MODERATE | c.46G>A|p.Val16Ile |
S134 |
| 163955 | BAA02g10600 | A02 | 4712402 | G | A | upstream_gene_variant | MODIFIER | c.-1977G>A| |
S274 |
| 163956 | BAA02g10600 | A02 | 4714840 | G | A | missense_variant | MODERATE | c.94G>A|p.Asp32Asn |
S156 |
| 163957 | BAA02g10600 | A02 | 4715041 | G | A | missense_variant | MODERATE | c.295G>A|p.Asp99Asn |
S210 S225 |
| 163958 | BAA02g10600 | A02 | 4715204 | C | T | missense_variant | MODERATE | c.458C>T|p.Pro153Leu |
S47 |
| 163959 | BAA02g10600 | A02 | 4715242 | G | A | missense_variant | MODERATE | c.496G>A|p.Asp166Asn |
S245 |
| 163960 | BAA02g10600 | A02 | 4715777 | G | A | missense_variant | MODERATE | c.724G>A|p.Ala242Thr |
S146 |
| 163961 | BAA02g10600 | A02 | 4715813 | C | T | missense_variant | MODERATE | c.760C>T|p.Pro254Ser |
S123 |
| 163962 | BAA02g10600 | A02 | 4715941 | G | A | synonymous_variant | LOW | c.888G>A|p.Lys296Lys |
S48 |
| 163963 | BAA02g10590 | A02 | 4716449 | G | A | downstream_gene_variant | MODIFIER | c.*3175G>A| |
S191 |
| 163964 | BAA02g10610 | A02 | 4717083 | C | T | synonymous_variant | LOW | c.1059G>A|p.Ala353Ala |
S270 |
| 163965 | BAA02g10610 | A02 | 4717313 | C | T | missense_variant | MODERATE | c.916G>A|p.Val306Ile |
S240 |
| 163966 | BAA02g10610 | A02 | 4718997 | C | T | upstream_gene_variant | MODIFIER | c.-769G>A| |
S121 |
| 163967 | BAA02g10610 | A02 | 4719613 | G | A | upstream_gene_variant | MODIFIER | c.-1385C>T| |
S294 |
| 163968 | BAA02g10610 | A02 | 4719688 | G | A | upstream_gene_variant | MODIFIER | c.-1460C>T| |
S12 |
| 163969 | BAA02g10610 | A02 | 4719948 | C | T | upstream_gene_variant | MODIFIER | c.-1720G>A| |
S183 S198 |
| 163970 | BAA02g10620 | A02 | 4721126 | C | T | missense_variant | MODERATE | c.593G>A|p.Ser198Asn |
S180 |
| 163971 | BAA02g10620 | A02 | 4721517 | C | T | missense_variant | MODERATE | c.202G>A|p.Asp68Asn |
S272 S273 |
| 163972 | BAA02g10630 | A02 | 4723009 | G | A | missense_variant | MODERATE | c.1439C>T|p.Pro480Leu |
S168 |
| 163973 | BAA02g10630 | A02 | 4723017 | G | A | synonymous_variant | LOW | c.1431C>T|p.Phe477Phe |
S52 |
| 163974 | BAA02g10620 | A02 | 4725526 | C | T | upstream_gene_variant | MODIFIER | c.-3808G>A| |
S218 S89 |
| 163975 | BAA02g10620 | A02 | 4725627 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S265 |