| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 129851 | BAA10g17590 | A10 | 16869752 | C | T | upstream_gene_variant | MODIFIER | c.-1667G>A| |
S176 |
| 129852 | BAA10g17590 | A10 | 16870105 | G | A | upstream_gene_variant | MODIFIER | c.-2020C>T| |
S217 |
| 129853 | BAA10g17590 | A10 | 16872229 | G | A | upstream_gene_variant | MODIFIER | c.-4144C>T| |
S236 |
| 129854 | BAA10g17590 | A10 | 16872797 | C | A | upstream_gene_variant | MODIFIER | c.-4712G>T| |
S296 |
| 129855 | BAA10g17590 | A10 | 16872798 | C | A | upstream_gene_variant | MODIFIER | c.-4713G>T| |
S16 |
| 129856 | BAA10g17590 | A10 | 16872852 | C | T | upstream_gene_variant | MODIFIER | c.-4767G>A| |
S37 |
| 129857 | BAA10g17590 | A10 | 16872958 | G | A | upstream_gene_variant | MODIFIER | c.-4873C>T| |
S57 |
| 129858 | BAA10g17600 | A10 | 16873582 | C | T | upstream_gene_variant | MODIFIER | c.-2266C>T| |
S103 |
| 129859 | BAA10g17600 | A10 | 16873963 | G | A | upstream_gene_variant | MODIFIER | c.-1885G>A| |
S181 |
| 129860 | BAA10g17600 | A10 | 16875417 | C | T | upstream_gene_variant | MODIFIER | c.-431C>T| |
S306 S308 |
| 129861 | BAA10g17600 | A10 | 16876145 | C | T | missense_variant | MODERATE | c.298C>T|p.His100Tyr |
S70 |
| 129862 | BAA10g17600 | A10 | 16876224 | C | T | missense_variant | MODERATE | c.377C>T|p.Thr126Met |
S162 |
| 129863 | BAA10g17600 | A10 | 16876944 | G | A | downstream_gene_variant | MODIFIER | c.*614G>A| |
S209 |
| 129864 | BAA10g17600 | A10 | 16877616 | C | T | downstream_gene_variant | MODIFIER | c.*1286C>T| |
S12 |
| 129865 | BAA10g17620 | A10 | 16877739 | G | A | upstream_gene_variant | MODIFIER | c.-4883G>A| |
S221 |
| 129866 | BAA10g17620 | A10 | 16878107 | C | T | upstream_gene_variant | MODIFIER | c.-4515C>T| |
S10 |
| 129867 | BAA10g17610 | A10 | 16878258 | C | T | missense_variant | MODERATE | c.610G>A|p.Ala204Thr |
S144 |
| 129868 | BAA10g17620 | A10 | 16879046 | G | A | upstream_gene_variant | MODIFIER | c.-3576G>A| |
S71 |
| 129869 | BAA10g17610 | A10 | 16880125 | G | T | upstream_gene_variant | MODIFIER | c.-436C>A| |
S216 |
| 129870 | BAA10g17610 | A10 | 16883710 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S221 |
| 129871 | BAA10g17610 | A10 | 16884647 | G | A | upstream_gene_variant | MODIFIER | c.-4958C>T| |
S1 S90 |
| 129872 | BAA10g17630 | A10 | 16884951 | G | A | upstream_gene_variant | MODIFIER | c.-4096G>A| |
S61 |
| 129873 | BAA10g17630 | A10 | 16885612 | C | T | upstream_gene_variant | MODIFIER | c.-3435C>T| |
S183 |
| 129874 | BAA10g17630 | A10 | 16886837 | G | A | upstream_gene_variant | MODIFIER | c.-2210G>A| |
S255 |
| 129875 | BAA10g17630 | A10 | 16887513 | G | A | upstream_gene_variant | MODIFIER | c.-1534G>A| |
S288 |