| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 134201 | BAA10g20410 | A10 | 18383535 | C | T | upstream_gene_variant | MODIFIER | c.-2012G>A| |
S92 |
| 134202 | BAA10g20420 | A10 | 18387035 | G | A | upstream_gene_variant | MODIFIER | c.-119C>T| |
S273 |
| 134203 | BAA10g20430 | A10 | 18389447 | C | T | missense_variant | MODERATE | c.466G>A|p.Glu156Lys |
S11 |
| 134204 | BAA10g20420 | A10 | 18391694 | G | A | upstream_gene_variant | MODIFIER | c.-4778C>T| |
S284 |
| 134205 | BAA10g20430 | A10 | 18392077 | G | A | upstream_gene_variant | MODIFIER | c.-64C>T| |
S274 |
| 134206 | BAA10g20430 | A10 | 18392569 | G | A | upstream_gene_variant | MODIFIER | c.-556C>T| |
S239 |
| 134207 | BAA10g20440 | A10 | 18393951 | G | A | missense_variant | MODERATE | c.250C>T|p.Leu84Phe |
S273 |
| 134208 | BAA10g20440 | A10 | 18394014 | C | T | missense_variant | MODERATE | c.187G>A|p.Gly63Arg |
S202 |
| 134209 | BAA10g20430 | A10 | 18395398 | G | A | upstream_gene_variant | MODIFIER | c.-3385C>T| |
S181 |
| 134210 | BAA10g20430 | A10 | 18396621 | C | T | upstream_gene_variant | MODIFIER | c.-4608G>A| |
S299 |
| 134211 | BAA10g20450 | A10 | 18398034 | G | A | missense_variant | MODERATE | c.457C>T|p.Pro153Ser |
S262 |
| 134212 | BAA10g20450 | A10 | 18400265 | G | A | synonymous_variant | LOW | c.42C>T|p.Asn14Asn |
S139 |
| 134213 | BAA10g20450 | A10 | 18401194 | C | T | upstream_gene_variant | MODIFIER | c.-888G>A| |
S78 S83 |
| 134214 | BAA10g20450 | A10 | 18401852 | C | T | upstream_gene_variant | MODIFIER | c.-1546G>A| |
S115 |
| 134215 | BAA10g20450 | A10 | 18402622 | G | A | upstream_gene_variant | MODIFIER | c.-2316C>T| |
S215 |
| 134216 | BAA10g20450 | A10 | 18403088 | G | A | upstream_gene_variant | MODIFIER | c.-2782C>T| |
S223 |
| 134217 | BAA10g20460 | A10 | 18403180 | C | T | synonymous_variant | LOW | c.786G>A|p.Lys262Lys |
S291 |
| 134218 | BAA10g20450 | A10 | 18404306 | G | A | upstream_gene_variant | MODIFIER | c.-4000C>T| |
S134 |
| 134219 | BAA10g20450 | A10 | 18404537 | G | A | upstream_gene_variant | MODIFIER | c.-4231C>T| |
S158 |
| 134220 | BAA10g20470 | A10 | 18405120 | G | A | missense_variant | MODERATE | c.1948C>T|p.Pro650Ser |
S67 |
| 134221 | BAA10g20470 | A10 | 18405770 | G | A | missense_variant | MODERATE | c.1457C>T|p.Ser486Phe |
S202 |
| 134222 | BAA10g20470 | A10 | 18406077 | G | A | missense_variant | MODERATE | c.1150C>T|p.Leu384Phe |
S136 |
| 134223 | BAA10g20460 | A10 | 18406253 | G | A | upstream_gene_variant | MODIFIER | c.-1746C>T| |
S176 |
| 134224 | BAA10g20470 | A10 | 18407265 | C | T | splice_region_variant&synonymous_variant | LOW | c.504G>A|p.Arg168Arg |
S142 |
| 134225 | BAA10g20470 | A10 | 18408561 | C | T | missense_variant | MODERATE | c.262G>A|p.Glu88Lys |
S114 |