| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 146901 | BAA10g31350 | A10 | 22899240 | G | A | synonymous_variant | LOW | c.1059G>A|p.Gln353Gln |
S106 S241 |
| 146902 | BAA10g31340 | A10 | 22899800 | C | T | upstream_gene_variant | MODIFIER | c.-3198G>A| |
S116 |
| 146903 | BAA10g31360 | A10 | 22901887 | G | A | upstream_gene_variant | MODIFIER | c.-3996G>A| |
S1 S90 |
| 146904 | BAA10g31360 | A10 | 22902351 | C | T | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S121 |
| 146905 | BAA10g31360 | A10 | 22903390 | C | T | upstream_gene_variant | MODIFIER | c.-2493C>T| |
S83 |
| 146906 | BAA10g31360 | A10 | 22905967 | G | A | missense_variant | MODERATE | c.85G>A|p.Glu29Lys |
S274 |
| 146907 | BAA10g31370 | A10 | 22906662 | C | T | downstream_gene_variant | MODIFIER | c.*4389G>A| |
S238 |
| 146908 | BAA10g31360 | A10 | 22907783 | G | A | downstream_gene_variant | MODIFIER | c.*50G>A| |
S202 |
| 146909 | BAA10g31360 | A10 | 22908535 | C | T | downstream_gene_variant | MODIFIER | c.*802C>T| |
S152 |
| 146910 | BAA10g31360 | A10 | 22908768 | C | T | downstream_gene_variant | MODIFIER | c.*1035C>T| |
S308 |
| 146911 | BAA10g31360 | A10 | 22908916 | G | A | downstream_gene_variant | MODIFIER | c.*1183G>A| |
S18 |
| 146912 | BAA10g31360 | A10 | 22908996 | G | A | downstream_gene_variant | MODIFIER | c.*1263G>A| |
S134 |
| 146913 | BAA10g31360 | A10 | 22909092 | G | A | downstream_gene_variant | MODIFIER | c.*1359G>A| |
S240 |
| 146914 | BAA10g31360 | A10 | 22909750 | C | T | downstream_gene_variant | MODIFIER | c.*2017C>T| |
S199 |
| 146915 | BAA10g31370 | A10 | 22911328 | C | T | missense_variant | MODERATE | c.364G>A|p.Asp122Asn |
S295 |
| 146916 | BAA10g31370 | A10 | 22911838 | G | A | synonymous_variant | LOW | c.58C>T|p.Leu20Leu |
S159 S243 |
| 146917 | BAA10g31380 | A10 | 22912693 | G | A | synonymous_variant | LOW | c.2166C>T|p.Ser722Ser |
S252 |
| 146918 | BAA10g31370 | A10 | 22913657 | G | A | upstream_gene_variant | MODIFIER | c.-1762C>T| |
S197 |
| 146919 | BAA10g31380 | A10 | 22913746 | C | T | missense_variant | MODERATE | c.1741G>A|p.Ala581Thr |
S135 |
| 146920 | BAA10g31380 | A10 | 22914900 | C | T | missense_variant | MODERATE | c.1058G>A|p.Arg353Lys |
S114 |
| 146921 | BAA10g31380 | A10 | 22915555 | C | T | synonymous_variant | LOW | c.609G>A|p.Leu203Leu |
S260 |
| 146922 | BAA10g31370 | A10 | 22916866 | G | A | upstream_gene_variant | MODIFIER | c.-4971C>T| |
S61 |
| 146923 | BAA10g31370 | A10 | 22916880 | C | T | upstream_gene_variant | MODIFIER | c.-4985G>A| |
S63 |
| 146924 | BAA10g31380 | A10 | 22917572 | C | T | upstream_gene_variant | MODIFIER | c.-962G>A| |
S19 |
| 146925 | BAA10g31380 | A10 | 22917798 | G | A | upstream_gene_variant | MODIFIER | c.-1188C>T| |
S57 |