| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144201 | BAA10g28860 | A10 | 21958571 | G | A | synonymous_variant | LOW | c.255C>T|p.Leu85Leu |
S64 |
| 144202 | BAA10g28860 | A10 | 21958732 | G | A | missense_variant | MODERATE | c.179C>T|p.Thr60Ile |
S118 |
| 144203 | BAA10g28850 | A10 | 21959503 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S125 |
| 144204 | BAA10g28870 | A10 | 21960127 | G | A | synonymous_variant | LOW | c.390G>A|p.Lys130Lys |
S64 |
| 144205 | BAA10g28870 | A10 | 21960149 | G | A | missense_variant | MODERATE | c.412G>A|p.Gly138Ser |
S42 |
| 144206 | BAA10g28880 | A10 | 21961916 | C | T | missense_variant | MODERATE | c.253C>T|p.Pro85Ser |
S251 |
| 144207 | BAA10g28890 | A10 | 21964605 | C | T | upstream_gene_variant | MODIFIER | c.-909C>T| |
S204 |
| 144208 | BAA10g28890 | A10 | 21965672 | G | A | synonymous_variant | LOW | c.159G>A|p.Glu53Glu |
S158 |
| 144209 | BAA10g28900 | A10 | 21967732 | C | T | upstream_gene_variant | MODIFIER | c.-1690C>T| |
S166 |
| 144210 | BAA10g28900 | A10 | 21968007 | G | A | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S132 S137 S215 S89 |
| 144211 | BAA10g28900 | A10 | 21968208 | G | A | upstream_gene_variant | MODIFIER | c.-1214G>A| |
S200 |
| 144212 | BAA10g28900 | A10 | 21969227 | G | A | upstream_gene_variant | MODIFIER | c.-195G>A| |
S203 |
| 144213 | BAA10g28900 | A10 | 21969566 | C | T | missense_variant | MODERATE | c.145C>T|p.Pro49Ser |
S56 |
| 144214 | BAA10g28890 | A10 | 21970519 | G | A | downstream_gene_variant | MODIFIER | c.*4613G>A| |
S134 |
| 144215 | BAA10g28900 | A10 | 21970951 | C | T | downstream_gene_variant | MODIFIER | c.*576C>T| |
S10 |
| 144216 | BAA10g28900 | A10 | 21972316 | T | C | downstream_gene_variant | MODIFIER | c.*1941T>C| |
S53 |
| 144217 | BAA10g28900 | A10 | 21972546 | G | A | downstream_gene_variant | MODIFIER | c.*2171G>A| |
S172 S217 |
| 144218 | BAA10g28910 | A10 | 21973532 | C | T | missense_variant | MODERATE | c.601G>A|p.Val201Ile |
S11 |
| 144219 | BAA10g28910 | A10 | 21973535 | A | C | missense_variant | MODERATE | c.598T>G|p.Leu200Val |
S17 S232 S246 S262 |
| 144220 | BAA10g28910 | A10 | 21973940 | C | T | missense_variant | MODERATE | c.193G>A|p.Asp65Asn |
S11 |
| 144221 | BAA10g28910 | A10 | 21974610 | G | A | upstream_gene_variant | MODIFIER | c.-478C>T| |
S126 |
| 144222 | BAA10g28910 | A10 | 21974669 | G | A | upstream_gene_variant | MODIFIER | c.-537C>T| |
S262 |
| 144223 | BAA10g28910 | A10 | 21975103 | G | A | upstream_gene_variant | MODIFIER | c.-971C>T| |
S184 |
| 144224 | BAA10g28910 | A10 | 21977492 | G | A | upstream_gene_variant | MODIFIER | c.-3360C>T| |
S85 |
| 144225 | BAA10g28920 | A10 | 21979208 | C | T | downstream_gene_variant | MODIFIER | c.*848G>A| |
S206 S26 |