Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
6001 | BAA01g04980 | A01 | 2198388 | G | A | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S54 |
6002 | BAA01g04980 | A01 | 2198856 | G | A | upstream_gene_variant | MODIFIER | c.-1438G>A| |
S8 |
6003 | BAA01g04980 | A01 | 2199309 | C | T | upstream_gene_variant | MODIFIER | c.-985C>T| |
S8 |
6004 | BAA01g04980 | A01 | 2199847 | C | T | upstream_gene_variant | MODIFIER | c.-447C>T| |
S64 |
6005 | BAA01g04980 | A01 | 2200153 | C | T | upstream_gene_variant | MODIFIER | c.-141C>T| |
S111 |
6006 | BAA01g04980 | A01 | 2200332 | G | A | synonymous_variant | LOW | c.39G>A|p.Lys13Lys |
S295 |
6007 | BAA01g04980 | A01 | 2200440 | T | A | synonymous_variant | LOW | c.147T>A|p.Leu49Leu |
S269 |
6008 | BAA01g04980 | A01 | 2200644 | C | T | missense_variant | MODERATE | c.256C>T|p.His86Tyr |
S48 |
6009 | BAA01g04980 | A01 | 2200869 | C | T | stop_gained | HIGH | c.481C>T|p.Gln161* |
S129 |
6010 | BAA01g04970 | A01 | 2202621 | C | T | downstream_gene_variant | MODIFIER | c.*4394C>T| |
S71 |
6011 | BAA01g04990 | A01 | 2203610 | C | T | missense_variant | MODERATE | c.902G>A|p.Ser301Asn |
S282 |
6012 | BAA01g04990 | A01 | 2203876 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.723-1G>A| |
S117 |
6013 | BAA01g05000 | A01 | 2204337 | G | A | upstream_gene_variant | MODIFIER | c.-4632G>A| |
S202 |
6014 | BAA01g05000 | A01 | 2205096 | G | A | upstream_gene_variant | MODIFIER | c.-3873G>A| |
S73 S91 |
6015 | BAA01g04990 | A01 | 2205613 | C | T | missense_variant | MODERATE | c.319G>A|p.Gly107Arg |
S35 |
6016 | BAA01g04990 | A01 | 2205756 | G | A | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S259 |
6017 | BAA01g04990 | A01 | 2205932 | C | T | upstream_gene_variant | MODIFIER | c.-1G>A| |
S18 |
6018 | BAA01g04990 | A01 | 2208770 | G | A | upstream_gene_variant | MODIFIER | c.-2839C>T| |
S294 |
6019 | BAA01g05000 | A01 | 2209937 | C | T | synonymous_variant | LOW | c.558C>T|p.Ser186Ser |
S260 |
6020 | BAA01g04990 | A01 | 2209999 | G | A | upstream_gene_variant | MODIFIER | c.-4068C>T| |
S108 |
6021 | BAA01g05000 | A01 | 2210049 | C | T | missense_variant | MODERATE | c.593C>T|p.Thr198Ile |
S205 |
6022 | BAA01g05000 | A01 | 2210677 | G | A | missense_variant | MODERATE | c.842G>A|p.Arg281His |
S172 S217 |
6023 | BAA01g05000 | A01 | 2211113 | G | A | missense_variant | MODERATE | c.1207G>A|p.Ala403Thr |
S72 S78 |
6024 | BAA01g05000 | A01 | 2211378 | G | A | missense_variant | MODERATE | c.1472G>A|p.Arg491Lys |
S156 |
6025 | BAA01g05000 | A01 | 2211531 | G | T | stop_gained | HIGH | c.1546G>T|p.Glu516* |
S250 |