| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 124651 | BAA10g14140 | A10 | 14965654 | G | A | missense_variant | MODERATE | c.1555C>T|p.Leu519Phe |
S109 |
| 124652 | BAA10g14140 | A10 | 14965821 | C | T | missense_variant | MODERATE | c.1388G>A|p.Ser463Asn |
S10 |
| 124653 | BAA10g14130 | A10 | 14966067 | C | T | downstream_gene_variant | MODIFIER | c.*832C>T| |
S200 |
| 124654 | BAA10g14130 | A10 | 14967413 | C | T | downstream_gene_variant | MODIFIER | c.*2178C>T| |
S48 |
| 124655 | BAA10g14140 | A10 | 14968734 | C | T | upstream_gene_variant | MODIFIER | c.-209G>A| |
S162 |
| 124656 | BAA10g14140 | A10 | 14969765 | C | T | upstream_gene_variant | MODIFIER | c.-1240G>A| |
S185 |
| 124657 | BAA10g14140 | A10 | 14970206 | C | T | upstream_gene_variant | MODIFIER | c.-1681G>A| |
S108 |
| 124658 | BAA10g14140 | A10 | 14971608 | C | T | upstream_gene_variant | MODIFIER | c.-3083G>A| |
S204 |
| 124659 | BAA10g14140 | A10 | 14971743 | T | C | upstream_gene_variant | MODIFIER | c.-3218A>G| |
S171 |
| 124660 | BAA10g14140 | A10 | 14971840 | G | A | upstream_gene_variant | MODIFIER | c.-3315C>T| |
S89 |
| 124661 | BAA10g14140 | A10 | 14973055 | G | A | upstream_gene_variant | MODIFIER | c.-4530C>T| |
S276 |
| 124662 | BAA10g14140 | A10 | 14973079 | G | A | upstream_gene_variant | MODIFIER | c.-4554C>T| |
S265 |
| 124663 | BAA10g14140 | A10 | 14973083 | G | A | upstream_gene_variant | MODIFIER | c.-4558C>T| |
S209 |
| 124664 | BAA10g14140 | A10 | 14973180 | G | A | upstream_gene_variant | MODIFIER | c.-4655C>T| |
S171 |
| 124665 | BAA10g14140 | A10 | 14973254 | G | A | upstream_gene_variant | MODIFIER | c.-4729C>T| |
S198 |
| 124666 | BAA10g14150 | A10 | 14975270 | C | T | upstream_gene_variant | MODIFIER | c.-3910G>A| |
S177 |
| 124667 | BAA10g14150 | A10 | 14975473 | G | A | upstream_gene_variant | MODIFIER | c.-4113C>T| |
S284 |
| 124668 | BAA10g14150 | A10 | 14975554 | G | A | upstream_gene_variant | MODIFIER | c.-4194C>T| |
S180 |
| 124669 | BAA10g14160 | A10 | 14976510 | G | A | downstream_gene_variant | MODIFIER | c.*704C>T| |
S262 |
| 124670 | BAA10g14160 | A10 | 14976807 | C | T | downstream_gene_variant | MODIFIER | c.*407G>A| |
S211 |
| 124671 | BAA10g14160 | A10 | 14976894 | G | A | downstream_gene_variant | MODIFIER | c.*320C>T| |
S59 |
| 124672 | BAA10g14160 | A10 | 14977679 | C | T | missense_variant | MODERATE | c.1306G>A|p.Asp436Asn |
S68 |
| 124673 | BAA10g14160 | A10 | 14977923 | G | A | synonymous_variant | LOW | c.1062C>T|p.Pro354Pro |
S10 |
| 124674 | BAA10g14160 | A10 | 14978732 | G | A | missense_variant | MODERATE | c.335C>T|p.Thr112Ile |
S90 |
| 124675 | BAA10g14160 | A10 | 14979569 | C | T | upstream_gene_variant | MODIFIER | c.-404G>A| |
S10 |