| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 134751 | BAA10g20860 | A10 | 18568462 | G | A | synonymous_variant | LOW | c.96C>T|p.Ser32Ser |
S64 |
| 134752 | BAA10g20860 | A10 | 18568482 | G | A | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S1 S90 |
| 134753 | BAA10g20870 | A10 | 18573724 | G | A | upstream_gene_variant | MODIFIER | c.-2237G>A| |
S138 |
| 134754 | BAA10g20870 | A10 | 18573993 | C | T | upstream_gene_variant | MODIFIER | c.-1968C>T| |
S117 |
| 134755 | BAA10g20870 | A10 | 18575170 | G | A | upstream_gene_variant | MODIFIER | c.-791G>A| |
S240 |
| 134756 | BAA10g20870 | A10 | 18576331 | C | T | missense_variant | MODERATE | c.371C>T|p.Ser124Phe |
S200 |
| 134757 | BAA10g20870 | A10 | 18576349 | C | T | missense_variant | MODERATE | c.389C>T|p.Thr130Ile |
S87 |
| 134758 | BAA10g20870 | A10 | 18576528 | G | A | intron_variant | MODIFIER | c.486+82G>A| |
S175 |
| 134759 | BAA10g20870 | A10 | 18576640 | G | A | missense_variant | MODERATE | c.499G>A|p.Asp167Asn |
S134 |
| 134760 | BAA10g20870 | A10 | 18576893 | C | T | missense_variant | MODERATE | c.752C>T|p.Ser251Phe |
S289 S290 |
| 134761 | BAA10g20870 | A10 | 18577938 | C | T | missense_variant | MODERATE | c.1672C>T|p.Leu558Phe |
S135 |
| 134762 | BAA10g20870 | A10 | 18578352 | A | C | missense_variant | MODERATE | c.2086A>C|p.Met696Leu |
S241 |
| 134763 | BAA10g20870 | A10 | 18578591 | C | T | synonymous_variant | LOW | c.2325C>T|p.Phe775Phe |
S84 S93 |
| 134764 | BAA10g20870 | A10 | 18578900 | C | T | synonymous_variant | LOW | c.2634C>T|p.Phe878Phe |
S294 |
| 134765 | BAA10g20870 | A10 | 18579111 | G | A | missense_variant | MODERATE | c.2845G>A|p.Glu949Lys |
S264 |
| 134766 | BAA10g20870 | A10 | 18579258 | G | A | missense_variant | MODERATE | c.2992G>A|p.Glu998Lys |
S202 |
| 134767 | BAA10g20870 | A10 | 18579437 | C | T | synonymous_variant | LOW | c.3171C>T|p.Asp1057Asp |
S99 |
| 134768 | BAA10g20870 | A10 | 18580145 | G | A | synonymous_variant | LOW | c.3879G>A|p.Arg1293Arg |
S203 |
| 134769 | BAA10g20870 | A10 | 18580308 | C | T | missense_variant | MODERATE | c.4042C>T|p.Leu1348Phe |
S183 |
| 134770 | BAA10g20880 | A10 | 18580492 | C | T | upstream_gene_variant | MODIFIER | c.-1225C>T| |
S44 |
| 134771 | BAA10g20880 | A10 | 18581893 | C | T | synonymous_variant | LOW | c.177C>T|p.Gly59Gly |
S86 |
| 134772 | BAA10g20880 | A10 | 18581941 | C | T | synonymous_variant | LOW | c.225C>T|p.Pro75Pro |
S56 |
| 134773 | BAA10g20890 | A10 | 18582502 | G | A | upstream_gene_variant | MODIFIER | c.-2277G>A| |
S223 |
| 134774 | BAA10g20890 | A10 | 18582558 | C | T | upstream_gene_variant | MODIFIER | c.-2221C>T| |
S92 |
| 134775 | BAA10g20890 | A10 | 18582684 | G | A | upstream_gene_variant | MODIFIER | c.-2095G>A| |
S132 S137 S215 S89 |