| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 139601 | BAA10g24800 | A10 | 20306515 | G | A | upstream_gene_variant | MODIFIER | c.-3742C>T| |
S9 |
| 139602 | BAA10g24800 | A10 | 20306699 | A | C | upstream_gene_variant | MODIFIER | c.-3926T>G| |
S172 S2 S26 S296 |
| 139603 | BAA10g24800 | A10 | 20306760 | G | A | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S120 |
| 139604 | BAA10g24800 | A10 | 20306771 | C | T | upstream_gene_variant | MODIFIER | c.-3998G>A| |
S255 |
| 139605 | BAA10g24800 | A10 | 20306802 | G | A | upstream_gene_variant | MODIFIER | c.-4029C>T| |
S159 S243 |
| 139606 | BAA10g24820 | A10 | 20308628 | G | A | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S32 |
| 139607 | BAA10g24820 | A10 | 20309280 | G | A | upstream_gene_variant | MODIFIER | c.-4218G>A| |
S190 |
| 139608 | BAA10g24810 | A10 | 20309952 | C | T | missense_variant | MODERATE | c.310G>A|p.Asp104Asn |
S292 |
| 139609 | BAA10g24810 | A10 | 20310614 | C | T | missense_variant | MODERATE | c.131G>A|p.Arg44Lys |
S135 |
| 139610 | BAA10g24820 | A10 | 20310770 | G | A | upstream_gene_variant | MODIFIER | c.-2728G>A| |
S276 |
| 139611 | BAA10g24810 | A10 | 20312903 | G | A | upstream_gene_variant | MODIFIER | c.-2018C>T| |
S100 |
| 139612 | BAA10g24810 | A10 | 20312909 | G | A | upstream_gene_variant | MODIFIER | c.-2024C>T| |
S67 |
| 139613 | BAA10g24810 | A10 | 20313107 | C | T | upstream_gene_variant | MODIFIER | c.-2222G>A| |
S188 |
| 139614 | BAA10g24820 | A10 | 20315250 | C | T | synonymous_variant | LOW | c.579C>T|p.His193His |
S84 S93 |
| 139615 | BAA10g24820 | A10 | 20315565 | C | T | missense_variant | MODERATE | c.770C>T|p.Ser257Phe |
S40 S49 |
| 139616 | BAA10g24820 | A10 | 20315578 | G | A | synonymous_variant | LOW | c.783G>A|p.Lys261Lys |
S63 |
| 139617 | BAA10g24820 | A10 | 20315681 | G | A | missense_variant | MODERATE | c.886G>A|p.Asp296Asn |
S184 |
| 139618 | BAA10g24830 | A10 | 20316457 | C | T | upstream_gene_variant | MODIFIER | c.-3406C>T| |
S177 |
| 139619 | BAA10g24830 | A10 | 20319030 | G | A | upstream_gene_variant | MODIFIER | c.-833G>A| |
S180 |
| 139620 | BAA10g24830 | A10 | 20319247 | C | T | upstream_gene_variant | MODIFIER | c.-616C>T| |
S40 S49 |
| 139621 | BAA10g24820 | A10 | 20320618 | G | A | downstream_gene_variant | MODIFIER | c.*4235G>A| |
S43 |
| 139622 | BAA10g24820 | A10 | 20320857 | G | A | downstream_gene_variant | MODIFIER | c.*4474G>A| |
S120 |
| 139623 | BAA10g24840 | A10 | 20321941 | G | A | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S286 |
| 139624 | BAA10g24840 | A10 | 20321987 | C | T | upstream_gene_variant | MODIFIER | c.-4858C>T| |
S155 |
| 139625 | BAA10g24840 | A10 | 20322081 | C | A | upstream_gene_variant | MODIFIER | c.-4764C>A| |
S305 |