| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 142701 | BAA10g27530 | A10 | 21434869 | C | T | missense_variant | MODERATE | c.1019G>A|p.Arg340Lys |
S176 |
| 142702 | BAA10g27530 | A10 | 21435159 | G | A | synonymous_variant | LOW | c.828C>T|p.Asn276Asn |
S212 |
| 142703 | BAA10g27520 | A10 | 21435422 | G | A | upstream_gene_variant | MODIFIER | c.-4743C>T| |
S118 |
| 142704 | BAA10g27540 | A10 | 21436722 | T | C | upstream_gene_variant | MODIFIER | c.-1436T>C| |
S274 |
| 142705 | BAA10g27540 | A10 | 21436789 | C | T | upstream_gene_variant | MODIFIER | c.-1369C>T| |
S247 |
| 142706 | BAA10g27540 | A10 | 21436960 | C | T | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S72 S78 |
| 142707 | BAA10g27530 | A10 | 21437433 | C | T | missense_variant | MODERATE | c.76G>A|p.Asp26Asn |
S211 |
| 142708 | BAA10g27530 | A10 | 21437439 | C | T | missense_variant | MODERATE | c.70G>A|p.Val24Ile |
S133 |
| 142709 | BAA10g27530 | A10 | 21437832 | G | A | upstream_gene_variant | MODIFIER | c.-324C>T| |
S263 |
| 142710 | BAA10g27540 | A10 | 21438179 | G | A | missense_variant | MODERATE | c.22G>A|p.Glu8Lys |
S205 |
| 142711 | BAA10g27540 | A10 | 21438831 | G | A | missense_variant | MODERATE | c.282G>A|p.Met94Ile |
S113 |
| 142712 | BAA10g27540 | A10 | 21439158 | G | A | missense_variant | MODERATE | c.524G>A|p.Gly175Asp |
S140 S278 S64 |
| 142713 | BAA10g27530 | A10 | 21439755 | G | A | upstream_gene_variant | MODIFIER | c.-2247C>T| |
S279 |
| 142714 | BAA10g27530 | A10 | 21439823 | G | A | upstream_gene_variant | MODIFIER | c.-2315C>T| |
S88 |
| 142715 | BAA10g27530 | A10 | 21439864 | G | A | upstream_gene_variant | MODIFIER | c.-2356C>T| |
S172 S217 |
| 142716 | BAA10g27550 | A10 | 21440517 | C | T | missense_variant | MODERATE | c.25C>T|p.Leu9Phe |
S36 |
| 142717 | BAA10g27530 | A10 | 21441529 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S153 S213 |
| 142718 | BAA10g27560 | A10 | 21441899 | G | A | missense_variant | MODERATE | c.266C>T|p.Ser89Phe |
S43 |
| 142719 | BAA10g27560 | A10 | 21442978 | G | A | upstream_gene_variant | MODIFIER | c.-449C>T| |
S180 |
| 142720 | BAA10g27560 | A10 | 21443623 | G | A | upstream_gene_variant | MODIFIER | c.-1094C>T| |
S66 |
| 142721 | BAA10g27560 | A10 | 21445224 | C | T | upstream_gene_variant | MODIFIER | c.-2695G>A| |
S247 |
| 142722 | BAA10g27560 | A10 | 21446187 | C | T | upstream_gene_variant | MODIFIER | c.-3658G>A| |
S255 |
| 142723 | BAA10g27580 | A10 | 21447838 | C | T | upstream_gene_variant | MODIFIER | c.-1978C>T| |
S264 |
| 142724 | BAA10g27570 | A10 | 21448139 | G | A | missense_variant&splice_region_variant | MODERATE | c.505G>A|p.Gly169Arg |
S271 |
| 142725 | BAA10g27570 | A10 | 21448164 | C | T | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S247 |