| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 112851 | BAA10g08650 | A10 | 10611164 | C | T | downstream_gene_variant | MODIFIER | c.*1825G>A| |
S133 |
| 112852 | BAA10g08650 | A10 | 10611821 | G | A | downstream_gene_variant | MODIFIER | c.*1168C>T| |
S105 S106 |
| 112853 | BAA10g08650 | A10 | 10611847 | G | A | downstream_gene_variant | MODIFIER | c.*1142C>T| |
S302 |
| 112854 | BAA10g08650 | A10 | 10612117 | C | T | downstream_gene_variant | MODIFIER | c.*872G>A| |
S235 |
| 112855 | BAA10g08650 | A10 | 10612562 | C | T | downstream_gene_variant | MODIFIER | c.*427G>A| |
S41 |
| 112856 | BAA10g08650 | A10 | 10614323 | G | A | missense_variant | MODERATE | c.2095C>T|p.Leu699Phe |
S283 |
| 112857 | BAA10g08650 | A10 | 10614612 | G | A | stop_gained | HIGH | c.1918C>T|p.Gln640* |
S217 |
| 112858 | BAA10g08650 | A10 | 10614950 | C | T | synonymous_variant | LOW | c.1725G>A|p.Gln575Gln |
S92 |
| 112859 | BAA10g08650 | A10 | 10615331 | G | A | missense_variant | MODERATE | c.1447C>T|p.Leu483Phe |
S295 |
| 112860 | BAA10g08650 | A10 | 10615895 | C | T | missense_variant | MODERATE | c.883G>A|p.Glu295Lys |
S183 |
| 112861 | BAA10g08650 | A10 | 10617381 | G | A | upstream_gene_variant | MODIFIER | c.-252C>T| |
S172 |
| 112862 | BAA10g08650 | A10 | 10617931 | G | A | upstream_gene_variant | MODIFIER | c.-802C>T| |
S18 |
| 112863 | BAA10g08650 | A10 | 10618175 | C | T | upstream_gene_variant | MODIFIER | c.-1046G>A| |
S162 |
| 112864 | BAA10g08650 | A10 | 10619240 | G | A | upstream_gene_variant | MODIFIER | c.-2111C>T| |
S65 |
| 112865 | BAA10g08650 | A10 | 10620062 | C | T | upstream_gene_variant | MODIFIER | c.-2933G>A| |
S246 |
| 112866 | BAA10g08650 | A10 | 10621181 | G | A | upstream_gene_variant | MODIFIER | c.-4052C>T| |
S237 |
| 112867 | BAA10g08660 | A10 | 10622876 | G | A | intron_variant | MODIFIER | c.152-102G>A| |
S43 |
| 112868 | BAA10g08660 | A10 | 10622923 | G | A | intron_variant | MODIFIER | c.152-55G>A| |
S241 |
| 112869 | BAA10g08660 | A10 | 10623170 | C | T | missense_variant | MODERATE | c.344C>T|p.Ser115Phe |
S143 |
| 112870 | BAA10g08660 | A10 | 10623192 | C | T | synonymous_variant | LOW | c.366C>T|p.Ala122Ala |
S162 |
| 112871 | BAA10g08660 | A10 | 10623497 | C | T | downstream_gene_variant | MODIFIER | c.*32C>T| |
S156 |
| 112872 | BAA10g08660 | A10 | 10623767 | G | A | downstream_gene_variant | MODIFIER | c.*302G>A| |
S139 |
| 112873 | BAA10g08660 | A10 | 10623857 | G | A | downstream_gene_variant | MODIFIER | c.*392G>A| |
S264 |
| 112874 | BAA10g08660 | A10 | 10624065 | G | A | downstream_gene_variant | MODIFIER | c.*600G>A| |
S198 |
| 112875 | BAA10g08660 | A10 | 10624106 | C | T | downstream_gene_variant | MODIFIER | c.*641C>T| |
S146 |