| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144001 | BAA10g28700 | A10 | 21901053 | G | A | upstream_gene_variant | MODIFIER | c.-1791C>T| |
S192 |
| 144002 | BAA10g28700 | A10 | 21901344 | C | T | upstream_gene_variant | MODIFIER | c.-2082G>A| |
S221 |
| 144003 | BAA10g28710 | A10 | 21904036 | A | G | synonymous_variant | LOW | c.294T>C|p.Thr98Thr |
S187 |
| 144004 | BAA10g28710 | A10 | 21904125 | G | A | stop_gained | HIGH | c.205C>T|p.Gln69* |
S109 |
| 144005 | BAA10g28710 | A10 | 21906312 | G | A | upstream_gene_variant | MODIFIER | c.-1983C>T| |
S230 |
| 144006 | BAA10g28710 | A10 | 21907275 | C | T | upstream_gene_variant | MODIFIER | c.-2946G>A| |
S148 S30 S31 |
| 144007 | BAA10g28720 | A10 | 21907354 | C | T | missense_variant | MODERATE | c.20C>T|p.Ser7Phe |
S157 S163 |
| 144008 | BAA10g28710 | A10 | 21907758 | C | T | upstream_gene_variant | MODIFIER | c.-3429G>A| |
S103 |
| 144009 | BAA10g28720 | A10 | 21908666 | C | T | missense_variant | MODERATE | c.935C>T|p.Pro312Leu |
S229 |
| 144010 | BAA10g28720 | A10 | 21908946 | C | T | missense_variant | MODERATE | c.1138C>T|p.Leu380Phe |
S104 S52 |
| 144011 | BAA10g28710 | A10 | 21909270 | C | T | upstream_gene_variant | MODIFIER | c.-4941G>A| |
S8 |
| 144012 | BAA10g28720 | A10 | 21909691 | G | A | downstream_gene_variant | MODIFIER | c.*734G>A| |
S138 |
| 144013 | BAA10g28720 | A10 | 21909949 | G | A | downstream_gene_variant | MODIFIER | c.*992G>A| |
S219 S72 |
| 144014 | BAA10g28740 | A10 | 21911951 | G | A | upstream_gene_variant | MODIFIER | c.-4816G>A| |
S108 |
| 144015 | BAA10g28740 | A10 | 21912564 | G | A | upstream_gene_variant | MODIFIER | c.-4203G>A| |
S293 |
| 144016 | BAA10g28740 | A10 | 21912839 | C | T | upstream_gene_variant | MODIFIER | c.-3928C>T| |
S129 |
| 144017 | BAA10g28740 | A10 | 21912857 | C | T | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S13 |
| 144018 | BAA10g28740 | A10 | 21913226 | C | T | upstream_gene_variant | MODIFIER | c.-3541C>T| |
S166 |
| 144019 | BAA10g28730 | A10 | 21913447 | C | T | missense_variant | MODERATE | c.1450G>A|p.Asp484Asn |
S97 |
| 144020 | BAA10g28730 | A10 | 21913608 | G | A | missense_variant | MODERATE | c.1289C>T|p.Ser430Leu |
S75 S81 |
| 144021 | BAA10g28730 | A10 | 21913721 | C | T | synonymous_variant | LOW | c.1176G>A|p.Glu392Glu |
S182 |
| 144022 | BAA10g28730 | A10 | 21914516 | G | A | missense_variant | MODERATE | c.709C>T|p.Arg237Cys |
S278 |
| 144023 | BAA10g28730 | A10 | 21915067 | G | A | missense_variant | MODERATE | c.158C>T|p.Ser53Phe |
S18 |
| 144024 | BAA10g28730 | A10 | 21915162 | G | A | synonymous_variant | LOW | c.63C>T|p.Ser21Ser |
S100 |
| 144025 | BAA10g28730 | A10 | 21915810 | G | A | upstream_gene_variant | MODIFIER | c.-586C>T| |
S240 |