| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 104301 | BAA10g07950 | A10 | 5033702 | C | T | missense_variant | MODERATE | c.392G>A|p.Arg131Gln |
S70 |
| 104302 | BAA10g07940 | A10 | 5034091 | G | A | upstream_gene_variant | MODIFIER | c.-3000C>T| |
S112 |
| 104303 | BAA10g07940 | A10 | 5034868 | C | T | upstream_gene_variant | MODIFIER | c.-3777G>A| |
S185 |
| 104304 | BAA10g07940 | A10 | 5035177 | C | T | upstream_gene_variant | MODIFIER | c.-4086G>A| |
S235 |
| 104305 | BAA10g07950 | A10 | 5037175 | C | T | upstream_gene_variant | MODIFIER | c.-2650G>A| |
S38 |
| 104306 | BAA10g07950 | A10 | 5039415 | C | T | upstream_gene_variant | MODIFIER | c.-4890G>A| |
S201 |
| 104307 | BAA10g07960 | A10 | 5039654 | C | T | upstream_gene_variant | MODIFIER | c.-1642C>T| |
S259 |
| 104308 | BAA10g07960 | A10 | 5039976 | C | T | upstream_gene_variant | MODIFIER | c.-1320C>T| |
S225 S73 |
| 104309 | BAA10g07960 | A10 | 5040811 | G | A | upstream_gene_variant | MODIFIER | c.-485G>A| |
S223 |
| 104310 | BAA10g07960 | A10 | 5041249 | G | A | upstream_gene_variant | MODIFIER | c.-47G>A| |
S163 |
| 104311 | BAA10g07960 | A10 | 5041361 | G | A | synonymous_variant | LOW | c.66G>A|p.Leu22Leu |
S43 |
| 104312 | BAA10g07970 | A10 | 5041530 | C | T | downstream_gene_variant | MODIFIER | c.*1791G>A| |
S282 |
| 104313 | BAA10g07960 | A10 | 5042107 | G | A | missense_variant | MODERATE | c.580G>A|p.Glu194Lys |
S219 S72 |
| 104314 | BAA10g07960 | A10 | 5043233 | G | A | downstream_gene_variant | MODIFIER | c.*555G>A| |
S221 |
| 104315 | BAA10g07970 | A10 | 5043443 | C | T | missense_variant | MODERATE | c.2188G>A|p.Gly730Ser |
S19 |
| 104316 | BAA10g07970 | A10 | 5043597 | C | T | synonymous_variant | LOW | c.2034G>A|p.Gly678Gly |
S301 S304 |
| 104317 | BAA10g07970 | A10 | 5044942 | G | A | splice_region_variant&intron_variant | LOW | c.1200+5C>T| |
S198 |
| 104318 | BAA10g07970 | A10 | 5044976 | G | A | missense_variant | MODERATE | c.1171C>T|p.Leu391Phe |
S20 |
| 104319 | BAA10g07970 | A10 | 5045164 | C | T | missense_variant | MODERATE | c.1084G>A|p.Val362Ile |
S150 |
| 104320 | BAA10g07970 | A10 | 5046322 | G | A | synonymous_variant | LOW | c.240C>T|p.Phe80Phe |
S207 |
| 104321 | BAA10g07970 | A10 | 5046565 | C | T | upstream_gene_variant | MODIFIER | c.-4G>A| |
S135 |
| 104322 | BAA10g07970 | A10 | 5048046 | G | A | upstream_gene_variant | MODIFIER | c.-1485C>T| |
S43 |
| 104323 | BAA10g07970 | A10 | 5048163 | C | T | upstream_gene_variant | MODIFIER | c.-1602G>A| |
S132 S137 S215 |
| 104324 | BAA10g07970 | A10 | 5049050 | G | A | upstream_gene_variant | MODIFIER | c.-2489C>T| |
S293 |
| 104325 | BAA10g07970 | A10 | 5049128 | C | T | upstream_gene_variant | MODIFIER | c.-2567G>A| |
S88 |