| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 52751 | BAA01g29120 | A01 | 18350181 | C | T | downstream_gene_variant | MODIFIER | c.*1656C>T| |
S242 |
| 52752 | BAA01g29120 | A01 | 18350298 | C | T | downstream_gene_variant | MODIFIER | c.*1773C>T| |
S136 |
| 52753 | BAA01g29120 | A01 | 18351308 | G | A | downstream_gene_variant | MODIFIER | c.*2783G>A| |
S292 |
| 52754 | BAA01g29130 | A01 | 18352942 | G | A | splice_region_variant&intron_variant | LOW | c.7679-7C>T| |
S57 |
| 52755 | BAA01g29130 | A01 | 18353542 | C | T | stop_gained | HIGH | c.7260G>A|p.Trp2420* |
S303 |
| 52756 | BAA01g29130 | A01 | 18353712 | C | T | splice_donor_variant&intron_variant | HIGH | c.7161+1G>A| |
S205 |
| 52757 | BAA01g29130 | A01 | 18353815 | C | T | synonymous_variant | LOW | c.7059G>A|p.Glu2353Glu |
S235 |
| 52758 | BAA01g29130 | A01 | 18354146 | G | A | missense_variant | MODERATE | c.6812C>T|p.Ser2271Phe |
S202 |
| 52759 | BAA01g29130 | A01 | 18357952 | C | T | missense_variant | MODERATE | c.4720G>A|p.Asp1574Asn |
S118 |
| 52760 | BAA01g29130 | A01 | 18358371 | C | T | missense_variant | MODERATE | c.4301G>A|p.Gly1434Glu |
S182 |
| 52761 | BAA01g29130 | A01 | 18358464 | C | T | missense_variant | MODERATE | c.4208G>A|p.Arg1403Lys |
S59 |
| 52762 | BAA01g29130 | A01 | 18358708 | C | T | missense_variant | MODERATE | c.3964G>A|p.Asp1322Asn |
S289 S290 |
| 52763 | BAA01g29130 | A01 | 18358809 | G | A | missense_variant | MODERATE | c.3863C>T|p.Ser1288Phe |
S100 |
| 52764 | BAA01g29130 | A01 | 18358839 | C | T | missense_variant | MODERATE | c.3833G>A|p.Arg1278Lys |
S183 |
| 52765 | BAA01g29130 | A01 | 18359651 | G | A | missense_variant | MODERATE | c.3143C>T|p.Ala1048Val |
S33 |
| 52766 | BAA01g29130 | A01 | 18359730 | C | T | missense_variant | MODERATE | c.3064G>A|p.Gly1022Ser |
S59 |
| 52767 | BAA01g29130 | A01 | 18359839 | C | T | synonymous_variant | LOW | c.2955G>A|p.Gln985Gln |
S94 |
| 52768 | BAA01g29130 | A01 | 18359959 | G | A | synonymous_variant | LOW | c.2835C>T|p.Asn945Asn |
S172 S217 |
| 52769 | BAA01g29130 | A01 | 18360143 | G | A | missense_variant | MODERATE | c.2651C>T|p.Pro884Leu |
S68 |
| 52770 | BAA01g29130 | A01 | 18360588 | C | T | missense_variant | MODERATE | c.2206G>A|p.Ala736Thr |
S42 |
| 52771 | BAA01g29130 | A01 | 18361072 | C | T | synonymous_variant | LOW | c.1722G>A|p.Lys574Lys |
S223 |
| 52772 | BAA01g29130 | A01 | 18362816 | C | T | missense_variant | MODERATE | c.781G>A|p.Asp261Asn |
S11 |
| 52773 | BAA01g29130 | A01 | 18363184 | C | T | missense_variant | MODERATE | c.575G>A|p.Arg192His |
S146 |
| 52774 | BAA01g29130 | A01 | 18363290 | C | T | missense_variant | MODERATE | c.469G>A|p.Glu157Lys |
S231 |
| 52775 | BAA01g29130 | A01 | 18363600 | C | T | missense_variant | MODERATE | c.271G>A|p.Asp91Asn |
S277 |