| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 116651 | BAA10g10380 | A10 | 12122567 | C | T | upstream_gene_variant | MODIFIER | c.-717C>T| |
S42 |
| 116652 | BAA10g10380 | A10 | 12123249 | C | T | upstream_gene_variant | MODIFIER | c.-35C>T| |
S136 S186 |
| 116653 | BAA10g10380 | A10 | 12123414 | C | T | missense_variant | MODERATE | c.131C>T|p.Ser44Phe |
S97 |
| 116654 | BAA10g10380 | A10 | 12123573 | C | T | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S243 S298 S299 |
| 116655 | BAA10g10380 | A10 | 12124103 | G | A | missense_variant | MODERATE | c.820G>A|p.Ala274Thr |
S284 |
| 116656 | BAA10g10380 | A10 | 12124348 | C | T | synonymous_variant | LOW | c.1065C>T|p.Leu355Leu |
S301 S304 |
| 116657 | BAA10g10380 | A10 | 12124383 | C | T | missense_variant | MODERATE | c.1100C>T|p.Thr367Ile |
S165 S211 S227 |
| 116658 | BAA10g10390 | A10 | 12132875 | G | A | downstream_gene_variant | MODIFIER | c.*4168C>T| |
S4 |
| 116659 | BAA10g10390 | A10 | 12133266 | C | T | downstream_gene_variant | MODIFIER | c.*3777G>A| |
S294 |
| 116660 | BAA10g10390 | A10 | 12133406 | C | T | downstream_gene_variant | MODIFIER | c.*3637G>A| |
S259 |
| 116661 | BAA10g10390 | A10 | 12133881 | G | A | downstream_gene_variant | MODIFIER | c.*3162C>T| |
S278 |
| 116662 | BAA10g10390 | A10 | 12133944 | C | T | downstream_gene_variant | MODIFIER | c.*3099G>A| |
S80 |
| 116663 | BAA10g10390 | A10 | 12134021 | G | A | downstream_gene_variant | MODIFIER | c.*3022C>T| |
S255 |
| 116664 | BAA10g10390 | A10 | 12134106 | C | T | downstream_gene_variant | MODIFIER | c.*2937G>A| |
S157 |
| 116665 | BAA10g10390 | A10 | 12134835 | C | T | downstream_gene_variant | MODIFIER | c.*2208G>A| |
S247 |
| 116666 | BAA10g10390 | A10 | 12135624 | G | A | downstream_gene_variant | MODIFIER | c.*1419C>T| |
S109 |
| 116667 | BAA10g10390 | A10 | 12137117 | C | T | missense_variant | MODERATE | c.487G>A|p.Ala163Thr |
S185 |
| 116668 | BAA10g10390 | A10 | 12137200 | C | T | missense_variant | MODERATE | c.404G>A|p.Gly135Glu |
S48 |
| 116669 | BAA10g10390 | A10 | 12137687 | G | A | missense_variant | MODERATE | c.95C>T|p.Thr32Ile |
S262 |
| 116670 | BAA10g10390 | A10 | 12138112 | G | A | upstream_gene_variant | MODIFIER | c.-96C>T| |
S207 |
| 116671 | BAA10g10400 | A10 | 12138409 | G | A | missense_variant | MODERATE | c.554C>T|p.Pro185Leu |
S207 |
| 116672 | BAA10g10400 | A10 | 12138480 | C | T | synonymous_variant | LOW | c.483G>A|p.Lys161Lys |
S37 |
| 116673 | BAA10g10390 | A10 | 12139281 | C | T | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S153 S213 |
| 116674 | BAA10g10390 | A10 | 12140476 | G | A | upstream_gene_variant | MODIFIER | c.-2460C>T| |
S221 |
| 116675 | BAA10g10390 | A10 | 12141219 | G | A | upstream_gene_variant | MODIFIER | c.-3203C>T| |
S234 |