| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 140201 | BAA10g25340 | A10 | 20522083 | G | A | upstream_gene_variant | MODIFIER | c.-292C>T| |
S71 |
| 140202 | BAA10g25340 | A10 | 20522267 | G | A | upstream_gene_variant | MODIFIER | c.-476C>T| |
S18 |
| 140203 | BAA10g25340 | A10 | 20522399 | C | T | upstream_gene_variant | MODIFIER | c.-608G>A| |
S56 |
| 140204 | BAA10g25350 | A10 | 20524358 | G | A | missense_variant | MODERATE | c.464G>A|p.Gly155Asp |
S293 |
| 140205 | BAA10g25350 | A10 | 20525357 | C | T | missense_variant | MODERATE | c.1376C>T|p.Ser459Phe |
S235 |
| 140206 | BAA10g25360 | A10 | 20526948 | G | A | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S272 |
| 140207 | BAA10g25360 | A10 | 20528195 | C | T | upstream_gene_variant | MODIFIER | c.-706C>T| |
S146 |
| 140208 | BAA10g25360 | A10 | 20528913 | G | A | missense_variant | MODERATE | c.13G>A|p.Gly5Arg |
S249 |
| 140209 | BAA10g25370 | A10 | 20532524 | C | T | upstream_gene_variant | MODIFIER | c.-1288C>T| |
S119 |
| 140210 | BAA10g25370 | A10 | 20532674 | G | A | upstream_gene_variant | MODIFIER | c.-1138G>A| |
S274 |
| 140211 | BAA10g25370 | A10 | 20533788 | G | A | upstream_gene_variant | MODIFIER | c.-24G>A| |
S74 |
| 140212 | BAA10g25370 | A10 | 20534150 | C | T | synonymous_variant | LOW | c.339C>T|p.Phe113Phe |
S18 |
| 140213 | BAA10g25380 | A10 | 20536345 | C | T | upstream_gene_variant | MODIFIER | c.-377C>T| |
S124 |
| 140214 | BAA10g25380 | A10 | 20536798 | C | T | missense_variant | MODERATE | c.77C>T|p.Ala26Val |
S157 S163 |
| 140215 | BAA10g25370 | A10 | 20536966 | G | A | downstream_gene_variant | MODIFIER | c.*1413G>A| |
S134 |
| 140216 | BAA10g25380 | A10 | 20537136 | C | T | synonymous_variant | LOW | c.327C>T|p.Thr109Thr |
S25 |
| 140217 | BAA10g25380 | A10 | 20537217 | G | A | synonymous_variant | LOW | c.408G>A|p.Arg136Arg |
S128 |
| 140218 | BAA10g25380 | A10 | 20537826 | C | T | missense_variant | MODERATE | c.485C>T|p.Ser162Phe |
S221 |
| 140219 | BAA10g25380 | A10 | 20538160 | C | T | synonymous_variant | LOW | c.819C>T|p.Leu273Leu |
S168 |
| 140220 | BAA10g25390 | A10 | 20539483 | C | T | missense_variant | MODERATE | c.1090G>A|p.Asp364Asn |
|
| 140221 | BAA10g25390 | A10 | 20539553 | G | A | synonymous_variant | LOW | c.1020C>T|p.Val340Val |
S286 |
| 140222 | BAA10g25390 | A10 | 20539927 | C | T | missense_variant | MODERATE | c.862G>A|p.Gly288Ser |
S197 |
| 140223 | BAA10g25400 | A10 | 20540567 | C | T | upstream_gene_variant | MODIFIER | c.-3282C>T| |
S8 |
| 140224 | BAA10g25390 | A10 | 20541894 | A | G | upstream_gene_variant | MODIFIER | c.-443T>C| |
S221 |
| 140225 | BAA10g25390 | A10 | 20544418 | G | A | upstream_gene_variant | MODIFIER | c.-2967C>T| |
S164 |