| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 93151 | BAA10g02680 | A10 | 1285920 | G | A | upstream_gene_variant | MODIFIER | c.-2601C>T| |
S203 |
| 93152 | BAA10g02680 | A10 | 1286098 | C | T | upstream_gene_variant | MODIFIER | c.-2779G>A| |
S133 |
| 93153 | BAA10g02680 | A10 | 1286124 | C | T | upstream_gene_variant | MODIFIER | c.-2805G>A| |
S31 |
| 93154 | BAA10g02680 | A10 | 1286251 | G | A | upstream_gene_variant | MODIFIER | c.-2932C>T| |
S128 |
| 93155 | BAA10g02680 | A10 | 1286403 | C | T | upstream_gene_variant | MODIFIER | c.-3084G>A| |
S31 |
| 93156 | BAA10g02680 | A10 | 1286425 | G | A | upstream_gene_variant | MODIFIER | c.-3106C>T| |
S219 S72 |
| 93157 | BAA10g02700 | A10 | 1289131 | G | A | missense_variant | MODERATE | c.217G>A|p.Glu73Lys |
S118 |
| 93158 | BAA10g02700 | A10 | 1289140 | G | A | missense_variant | MODERATE | c.226G>A|p.Gly76Arg |
S67 |
| 93159 | BAA10g02700 | A10 | 1289201 | G | A | missense_variant | MODERATE | c.287G>A|p.Gly96Glu |
S158 |
| 93160 | BAA10g02700 | A10 | 1289661 | G | A | synonymous_variant | LOW | c.747G>A|p.Glu249Glu |
S279 |
| 93161 | BAA10g02700 | A10 | 1289956 | G | A | missense_variant | MODERATE | c.1042G>A|p.Gly348Arg |
S156 S2 S3 S34 |
| 93162 | BAA10g02700 | A10 | 1290462 | G | A | synonymous_variant | LOW | c.1548G>A|p.Lys516Lys |
S245 |
| 93163 | BAA10g02690 | A10 | 1290824 | G | A | upstream_gene_variant | MODIFIER | c.-2319C>T| |
S36 |
| 93164 | BAA10g02710 | A10 | 1291275 | G | A | missense_variant | MODERATE | c.143C>T|p.Pro48Leu |
S241 |
| 93165 | BAA10g02690 | A10 | 1291987 | C | T | upstream_gene_variant | MODIFIER | c.-3482G>A| |
S287 |
| 93166 | BAA10g02720 | A10 | 1294514 | G | A | synonymous_variant | LOW | c.1668C>T|p.Asn556Asn |
S171 |
| 93167 | BAA10g02710 | A10 | 1295451 | C | T | upstream_gene_variant | MODIFIER | c.-4034G>A| |
S73 |
| 93168 | BAA10g02710 | A10 | 1295939 | C | T | upstream_gene_variant | MODIFIER | c.-4522G>A| |
S87 |
| 93169 | BAA10g02710 | A10 | 1296180 | G | A | upstream_gene_variant | MODIFIER | c.-4763C>T| |
S18 |
| 93170 | BAA10g02720 | A10 | 1297039 | G | A | intron_variant | MODIFIER | c.774+15C>T| |
S236 |
| 93171 | BAA10g02720 | A10 | 1297685 | G | A | intron_variant | MODIFIER | c.382+26C>T| |
S153 S213 |
| 93172 | BAA10g02720 | A10 | 1298165 | G | A | missense_variant | MODERATE | c.214C>T|p.Pro72Ser |
S296 |
| 93173 | BAA10g02720 | A10 | 1298648 | C | T | upstream_gene_variant | MODIFIER | c.-270G>A| |
S273 |
| 93174 | BAA10g02720 | A10 | 1298917 | G | A | upstream_gene_variant | MODIFIER | c.-539C>T| |
S274 |
| 93175 | BAA10g02720 | A10 | 1299916 | G | A | upstream_gene_variant | MODIFIER | c.-1538C>T| |
S241 |