| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150651 | BAA10g34590 | A10 | 24283358 | G | A | upstream_gene_variant | MODIFIER | c.-3404C>T| |
S125 |
| 150652 | BAA10g34590 | A10 | 24283374 | G | A | upstream_gene_variant | MODIFIER | c.-3420C>T| |
S79 S84 |
| 150653 | BAA10g34590 | A10 | 24283433 | G | A | upstream_gene_variant | MODIFIER | c.-3479C>T| |
S193 |
| 150654 | BAA10g34590 | A10 | 24283469 | C | T | upstream_gene_variant | MODIFIER | c.-3515G>A| |
S206 S26 |
| 150655 | BAA10g34620 | A10 | 24285174 | G | A | splice_region_variant&intron_variant | LOW | c.592+4G>A| |
S257 |
| 150656 | BAA10g34620 | A10 | 24285267 | C | T | missense_variant | MODERATE | c.599C>T|p.Ser200Phe |
S177 |
| 150657 | BAA10g34600 | A10 | 24285330 | C | T | upstream_gene_variant | MODIFIER | c.-3554G>A| |
S20 |
| 150658 | BAA10g34620 | A10 | 24285439 | C | T | synonymous_variant | LOW | c.684C>T|p.Asn228Asn |
S161 |
| 150659 | BAA10g34620 | A10 | 24286034 | G | A | missense_variant | MODERATE | c.1036G>A|p.Asp346Asn |
S57 |
| 150660 | BAA10g34630 | A10 | 24287665 | C | T | missense_variant | MODERATE | c.600G>A|p.Met200Ile |
S60 |
| 150661 | BAA10g34630 | A10 | 24288884 | C | T | upstream_gene_variant | MODIFIER | c.-301G>A| |
S176 |
| 150662 | BAA10g34630 | A10 | 24289955 | C | G | upstream_gene_variant | MODIFIER | c.-1372G>C| |
S196 |
| 150663 | BAA10g34630 | A10 | 24290958 | C | T | upstream_gene_variant | MODIFIER | c.-2375G>A| |
S247 |
| 150664 | BAA10g34630 | A10 | 24291315 | C | T | upstream_gene_variant | MODIFIER | c.-2732G>A| |
S292 |
| 150665 | BAA10g34630 | A10 | 24291781 | G | A | upstream_gene_variant | MODIFIER | c.-3198C>T| |
S9 |
| 150666 | BAA10g34650 | A10 | 24291917 | C | T | synonymous_variant | LOW | c.324G>A|p.Ser108Ser |
S190 |
| 150667 | BAA10g34630 | A10 | 24292944 | C | T | upstream_gene_variant | MODIFIER | c.-4361G>A| |
S36 |
| 150668 | BAA10g34630 | A10 | 24293424 | G | A | upstream_gene_variant | MODIFIER | c.-4841C>T| |
S7 |
| 150669 | BAA10g34630 | A10 | 24293456 | C | T | upstream_gene_variant | MODIFIER | c.-4873G>A| |
S105 |
| 150670 | BAA10g34640 | A10 | 24294782 | C | T | upstream_gene_variant | MODIFIER | c.-3516G>A| |
S135 |
| 150671 | BAA10g34660 | A10 | 24295578 | C | T | missense_variant | MODERATE | c.16C>T|p.Pro6Ser |
S13 |
| 150672 | BAA10g34640 | A10 | 24295826 | C | T | upstream_gene_variant | MODIFIER | c.-4560G>A| |
S67 |
| 150673 | BAA10g34640 | A10 | 24296129 | C | T | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S19 |
| 150674 | BAA10g34650 | A10 | 24296903 | G | A | upstream_gene_variant | MODIFIER | c.-4331C>T| |
S288 |
| 150675 | BAA10g34670 | A10 | 24298323 | C | T | upstream_gene_variant | MODIFIER | c.-198G>A| |
S89 |