| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144901 | BAA10g29560 | A10 | 22202075 | C | T | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S305 |
| 144902 | BAA10g29590 | A10 | 22202233 | C | T | upstream_gene_variant | MODIFIER | c.-2740C>T| |
S305 |
| 144903 | BAA10g29580 | A10 | 22203193 | C | T | synonymous_variant | LOW | c.498C>T|p.Ile166Ile |
S281 |
| 144904 | BAA10g29580 | A10 | 22203568 | G | A | missense_variant | MODERATE | c.727G>A|p.Asp243Asn |
S120 |
| 144905 | BAA10g29580 | A10 | 22203707 | C | A | missense_variant | MODERATE | c.866C>A|p.Ser289Tyr |
S306 S308 |
| 144906 | BAA10g29580 | A10 | 22203713 | G | A | missense_variant | MODERATE | c.872G>A|p.Gly291Glu |
S237 |
| 144907 | BAA10g29590 | A10 | 22206215 | G | A | synonymous_variant | LOW | c.609G>A|p.Leu203Leu |
S279 |
| 144908 | BAA10g29600 | A10 | 22207056 | C | T | upstream_gene_variant | MODIFIER | c.-3503C>T| |
S86 |
| 144909 | BAA10g29600 | A10 | 22207223 | C | T | upstream_gene_variant | MODIFIER | c.-3336C>T| |
S246 |
| 144910 | BAA10g29600 | A10 | 22207873 | C | T | upstream_gene_variant | MODIFIER | c.-2686C>T| |
S301 S304 |
| 144911 | BAA10g29600 | A10 | 22208479 | G | A | upstream_gene_variant | MODIFIER | c.-2080G>A| |
S125 |
| 144912 | BAA10g29600 | A10 | 22208791 | G | A | upstream_gene_variant | MODIFIER | c.-1768G>A| |
S223 |
| 144913 | BAA10g29600 | A10 | 22209189 | C | T | upstream_gene_variant | MODIFIER | c.-1370C>T| |
S112 |
| 144914 | BAA10g29600 | A10 | 22210648 | G | A | synonymous_variant | LOW | c.90G>A|p.Glu30Glu |
S298 |
| 144915 | BAA10g29600 | A10 | 22210707 | C | T | missense_variant | MODERATE | c.149C>T|p.Thr50Ile |
S259 |
| 144916 | BAA10g29600 | A10 | 22210747 | G | A | synonymous_variant | LOW | c.189G>A|p.Gln63Gln |
S298 |
| 144917 | BAA10g29600 | A10 | 22210826 | G | A | missense_variant | MODERATE | c.268G>A|p.Glu90Lys |
S251 |
| 144918 | BAA10g29590 | A10 | 22211142 | G | A | downstream_gene_variant | MODIFIER | c.*4268G>A| |
S209 |
| 144919 | BAA10g29600 | A10 | 22211531 | G | A | missense_variant | MODERATE | c.728G>A|p.Gly243Glu |
S263 |
| 144920 | BAA10g29600 | A10 | 22211703 | G | T | missense_variant | MODERATE | c.900G>T|p.Leu300Phe |
S197 |
| 144921 | BAA10g29600 | A10 | 22212198 | C | T | synonymous_variant | LOW | c.1395C>T|p.Leu465Leu |
S92 |
| 144922 | BAA10g29610 | A10 | 22213267 | G | A | downstream_gene_variant | MODIFIER | c.*4969C>T| |
S212 |
| 144923 | BAA10g29610 | A10 | 22213981 | C | T | downstream_gene_variant | MODIFIER | c.*4255G>A| |
S42 |
| 144924 | BAA10g29610 | A10 | 22214123 | G | A | downstream_gene_variant | MODIFIER | c.*4113C>T| |
S16 |
| 144925 | BAA10g29610 | A10 | 22214241 | G | A | downstream_gene_variant | MODIFIER | c.*3995C>T| |
S1 S90 |