| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 116851 | BAA10g10460 | A10 | 12191728 | G | A | upstream_gene_variant | MODIFIER | c.-4286G>A| |
S36 |
| 116852 | BAA10g10460 | A10 | 12191814 | C | T | upstream_gene_variant | MODIFIER | c.-4200C>T| |
S176 |
| 116853 | BAA10g10460 | A10 | 12194346 | G | A | upstream_gene_variant | MODIFIER | c.-1668G>A| |
S302 |
| 116854 | BAA10g10460 | A10 | 12194535 | C | T | upstream_gene_variant | MODIFIER | c.-1479C>T| |
S97 |
| 116855 | BAA10g10460 | A10 | 12194812 | C | T | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S247 |
| 116856 | BAA10g10460 | A10 | 12195258 | C | T | upstream_gene_variant | MODIFIER | c.-756C>T| |
S19 |
| 116857 | BAA10g10460 | A10 | 12195283 | C | T | upstream_gene_variant | MODIFIER | c.-731C>T| |
S28 |
| 116858 | BAA10g10460 | A10 | 12195506 | G | A | upstream_gene_variant | MODIFIER | c.-508G>A| |
S296 |
| 116859 | BAA10g10460 | A10 | 12196289 | C | T | synonymous_variant | LOW | c.276C>T|p.Phe92Phe |
S259 |
| 116860 | BAA10g10460 | A10 | 12196474 | C | T | missense_variant | MODERATE | c.461C>T|p.Ala154Val |
S162 |
| 116861 | BAA10g10460 | A10 | 12196771 | G | A | missense_variant | MODERATE | c.758G>A|p.Gly253Asp |
S172 S217 |
| 116862 | BAA10g10460 | A10 | 12197376 | C | T | downstream_gene_variant | MODIFIER | c.*46C>T| |
S272 |
| 116863 | BAA10g10470 | A10 | 12198180 | C | T | synonymous_variant | LOW | c.1476G>A|p.Lys492Lys |
S188 |
| 116864 | BAA10g10470 | A10 | 12200041 | C | T | missense_variant | MODERATE | c.307G>A|p.Glu103Lys |
S87 |
| 116865 | BAA10g10470 | A10 | 12200795 | C | T | upstream_gene_variant | MODIFIER | c.-267G>A| |
S246 |
| 116866 | BAA10g10470 | A10 | 12201763 | C | T | upstream_gene_variant | MODIFIER | c.-1235G>A| |
S270 |
| 116867 | BAA10g10470 | A10 | 12202022 | C | T | upstream_gene_variant | MODIFIER | c.-1494G>A| |
S145 S162 |
| 116868 | BAA10g10470 | A10 | 12202146 | C | T | upstream_gene_variant | MODIFIER | c.-1618G>A| |
S46 |
| 116869 | BAA10g10470 | A10 | 12202216 | C | T | upstream_gene_variant | MODIFIER | c.-1688G>A| |
S10 |
| 116870 | BAA10g10470 | A10 | 12202811 | C | T | upstream_gene_variant | MODIFIER | c.-2283G>A| |
S143 |
| 116871 | BAA10g10470 | A10 | 12203072 | C | T | upstream_gene_variant | MODIFIER | c.-2544G>A| |
S126 |
| 116872 | BAA10g10470 | A10 | 12203104 | G | A | upstream_gene_variant | MODIFIER | c.-2576C>T| |
S198 |
| 116873 | BAA10g10470 | A10 | 12203280 | C | T | upstream_gene_variant | MODIFIER | c.-2752G>A| |
S269 |
| 116874 | BAA10g10470 | A10 | 12203424 | C | T | upstream_gene_variant | MODIFIER | c.-2896G>A| |
S187 S243 S298 S299 |
| 116875 | BAA10g10470 | A10 | 12203669 | C | T | upstream_gene_variant | MODIFIER | c.-3141G>A| |
S233 |