| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 122551 | BAA10g12850 | A10 | 14173499 | C | T | upstream_gene_variant | MODIFIER | c.-3978C>T| |
S48 |
| 122552 | BAA10g12850 | A10 | 14173670 | C | T | upstream_gene_variant | MODIFIER | c.-3807C>T| |
S143 |
| 122553 | BAA10g12850 | A10 | 14174049 | G | A | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S61 |
| 122554 | BAA10g12850 | A10 | 14175041 | G | A | upstream_gene_variant | MODIFIER | c.-2436G>A| |
S201 |
| 122555 | BAA10g12840 | A10 | 14175605 | G | A | missense_variant | MODERATE | c.217C>T|p.Pro73Ser |
S72 |
| 122556 | BAA10g12840 | A10 | 14175743 | C | T | missense_variant | MODERATE | c.169G>A|p.Asp57Asn |
S98 |
| 122557 | BAA10g12840 | A10 | 14176012 | C | T | upstream_gene_variant | MODIFIER | c.-20G>A| |
S51 |
| 122558 | BAA10g12840 | A10 | 14176954 | C | T | upstream_gene_variant | MODIFIER | c.-962G>A| |
S92 |
| 122559 | BAA10g12840 | A10 | 14177179 | C | T | upstream_gene_variant | MODIFIER | c.-1187G>A| |
S232 |
| 122560 | BAA10g12850 | A10 | 14178267 | G | A | missense_variant | MODERATE | c.235G>A|p.Gly79Arg |
S65 |
| 122561 | BAA10g12850 | A10 | 14178954 | G | A | splice_region_variant&intron_variant | LOW | c.637+4G>A| |
S192 |
| 122562 | BAA10g12850 | A10 | 14179637 | C | T | missense_variant | MODERATE | c.1039C>T|p.Pro347Ser |
S269 |
| 122563 | BAA10g12850 | A10 | 14179706 | G | A | missense_variant | MODERATE | c.1108G>A|p.Val370Ile |
S240 |
| 122564 | BAA10g12850 | A10 | 14180346 | C | T | missense_variant | MODERATE | c.1289C>T|p.Pro430Leu |
S142 |
| 122565 | BAA10g12840 | A10 | 14180696 | C | T | upstream_gene_variant | MODIFIER | c.-4704G>A| |
S54 |
| 122566 | BAA10g12850 | A10 | 14181274 | C | T | missense_variant | MODERATE | c.1630C>T|p.Leu544Phe |
S247 |
| 122567 | BAA10g12850 | A10 | 14181794 | G | A | missense_variant | MODERATE | c.1933G>A|p.Asp645Asn |
S283 |
| 122568 | BAA10g12860 | A10 | 14182321 | C | T | upstream_gene_variant | MODIFIER | c.-298C>T| |
S156 |
| 122569 | BAA10g12860 | A10 | 14184662 | C | T | stop_gained | HIGH | c.838C>T|p.Gln280* |
S12 |
| 122570 | BAA10g12850 | A10 | 14185296 | C | T | downstream_gene_variant | MODIFIER | c.*3437C>T| |
S156 |
| 122571 | BAA10g12850 | A10 | 14185642 | G | A | downstream_gene_variant | MODIFIER | c.*3783G>A| |
S201 |
| 122572 | BAA10g12850 | A10 | 14186349 | C | T | downstream_gene_variant | MODIFIER | c.*4490C>T| |
S37 |
| 122573 | BAA10g12850 | A10 | 14186772 | T | C | downstream_gene_variant | MODIFIER | c.*4913T>C| |
S97 |
| 122574 | BAA10g12860 | A10 | 14187492 | G | A | downstream_gene_variant | MODIFIER | c.*1992G>A| |
S85 |
| 122575 | BAA10g12860 | A10 | 14187668 | G | A | downstream_gene_variant | MODIFIER | c.*2168G>A| |
S18 |