| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 129551 | BAA10g17450 | A10 | 16774897 | G | A | upstream_gene_variant | MODIFIER | c.-660G>A| |
S284 |
| 129552 | BAA10g17440 | A10 | 16775033 | G | A | synonymous_variant | LOW | c.375C>T|p.Leu125Leu |
S65 |
| 129553 | BAA10g17440 | A10 | 16775149 | G | A | missense_variant | MODERATE | c.259C>T|p.Leu87Phe |
S265 |
| 129554 | BAA10g17440 | A10 | 16775378 | C | T | stop_gained | HIGH | c.30G>A|p.Trp10* |
S296 |
| 129555 | BAA10g17440 | A10 | 16775445 | G | A | upstream_gene_variant | MODIFIER | c.-38C>T| |
S295 |
| 129556 | BAA10g17450 | A10 | 16775576 | G | A | missense_variant | MODERATE | c.20G>A|p.Arg7Gln |
S75 S81 |
| 129557 | BAA10g17440 | A10 | 16778317 | G | A | upstream_gene_variant | MODIFIER | c.-2910C>T| |
S293 |
| 129558 | BAA10g17440 | A10 | 16780361 | G | T | upstream_gene_variant | MODIFIER | c.-4954C>A| |
S181 |
| 129559 | BAA10g17450 | A10 | 16780751 | C | T | intron_variant | MODIFIER | c.654-1454C>T| |
S110 |
| 129560 | BAA10g17450 | A10 | 16780877 | C | T | intron_variant | MODIFIER | c.654-1328C>T| |
S42 |
| 129561 | BAA10g17450 | A10 | 16783059 | C | T | splice_region_variant&intron_variant | LOW | c.1346+6C>T| |
S282 |
| 129562 | BAA10g17450 | A10 | 16783120 | C | T | intron_variant | MODIFIER | c.1347-30C>T| |
S124 |
| 129563 | BAA10g17450 | A10 | 16784223 | C | T | intron_variant | MODIFIER | c.1418+1002C>T| |
S224 |
| 129564 | BAA10g17450 | A10 | 16784403 | G | A | intron_variant | MODIFIER | c.1419-1013G>A| |
S223 |
| 129565 | BAA10g17450 | A10 | 16785165 | C | T | intron_variant | MODIFIER | c.1419-251C>T| |
S122 |
| 129566 | BAA10g17450 | A10 | 16785787 | G | A | missense_variant | MODERATE | c.1702G>A|p.Gly568Ser |
S174 S27 |
| 129567 | BAA10g17450 | A10 | 16785981 | G | A | intron_variant | MODIFIER | c.1810-9G>A| |
S132 S215 S89 |
| 129568 | BAA10g17450 | A10 | 16786056 | G | A | missense_variant | MODERATE | c.1876G>A|p.Asp626Asn |
S72 S78 |
| 129569 | BAA10g17450 | A10 | 16786761 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2003-1G>A| |
S298 |
| 129570 | BAA10g17450 | A10 | 16790027 | C | T | synonymous_variant | LOW | c.2433C>T|p.Cys811Cys |
S143 S171 |
| 129571 | BAA10g17450 | A10 | 16790586 | C | T | synonymous_variant | LOW | c.2841C>T|p.Phe947Phe |
S25 |
| 129572 | BAA10g17450 | A10 | 16791008 | C | T | missense_variant | MODERATE | c.3115C>T|p.Leu1039Phe |
S45 |
| 129573 | BAA10g17450 | A10 | 16791508 | G | A | synonymous_variant | LOW | c.3615G>A|p.Lys1205Lys |
S261 |
| 129574 | BAA10g17460 | A10 | 16792398 | G | A | upstream_gene_variant | MODIFIER | c.-869G>A| |
S118 |
| 129575 | BAA10g17460 | A10 | 16792972 | C | T | upstream_gene_variant | MODIFIER | c.-295C>T| |
S142 |