Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g45450 | A03 | 21734787 | C | T | synonymous_variant | LOW | c.13644G>A|p.Lys4548Lys |
S202 |
2 | BAA03g45450 | A03 | 21734801 | C | T | missense_variant | MODERATE | c.13630G>A|p.Val4544Ile |
S18 |
3 | BAA03g45450 | A03 | 21735056 | G | A | stop_gained | HIGH | c.13375C>T|p.Gln4459* |
S95 |
4 | BAA03g45450 | A03 | 21735365 | C | T | missense_variant | MODERATE | c.13066G>A|p.Glu4356Lys |
S159 S243 |
5 | BAA03g45450 | A03 | 21735754 | G | A | missense_variant | MODERATE | c.12745C>T|p.Pro4249Ser |
S193 |
6 | BAA03g45450 | A03 | 21735984 | C | T | missense_variant | MODERATE | c.12515G>A|p.Arg4172His |
S35 |
7 | BAA03g45450 | A03 | 21737453 | C | T | missense_variant | MODERATE | c.11539G>A|p.Glu3847Lys |
S38 |
8 | BAA03g45450 | A03 | 21738114 | C | T | synonymous_variant | LOW | c.10878G>A|p.Glu3626Glu |
S183 S198 |
9 | BAA03g45450 | A03 | 21738236 | G | A | missense_variant | MODERATE | c.10756C>T|p.Pro3586Ser |
S105 S106 |
10 | BAA03g45450 | A03 | 21738290 | C | T | missense_variant | MODERATE | c.10702G>A|p.Asp3568Asn |
S120 |
11 | BAA03g45450 | A03 | 21741194 | G | A | intron_variant | MODIFIER | c.8759-28C>T| |
S28 |
12 | BAA03g45450 | A03 | 21742534 | G | A | stop_gained | HIGH | c.7762C>T|p.Arg2588* |
S36 |
13 | BAA03g45450 | A03 | 21742842 | G | A | missense_variant | MODERATE | c.7454C>T|p.Pro2485Leu |
S152 |
14 | BAA03g45450 | A03 | 21743169 | C | T | missense_variant | MODERATE | c.7127G>A|p.Gly2376Asp |
S209 |
15 | BAA03g45450 | A03 | 21744125 | G | A | missense_variant | MODERATE | c.6331C>T|p.Arg2111Cys |
S162 |
16 | BAA03g45450 | A03 | 21744449 | C | T | missense_variant | MODERATE | c.6007G>A|p.Glu2003Lys |
S99 |
17 | BAA03g45450 | A03 | 21744765 | T | C | synonymous_variant | LOW | c.5691A>G|p.Ala1897Ala |
S192 |
18 | BAA03g45450 | A03 | 21746350 | G | A | missense_variant | MODERATE | c.4106C>T|p.Ser1369Leu |
S168 |
19 | BAA03g45450 | A03 | 21747848 | C | T | missense_variant | MODERATE | c.2608G>A|p.Asp870Asn |
S172 S217 |
20 | BAA03g45450 | A03 | 21747963 | C | T | synonymous_variant | LOW | c.2493G>A|p.Thr831Thr |
S117 |
21 | BAA03g45450 | A03 | 21747970 | G | A | missense_variant | MODERATE | c.2486C>T|p.Thr829Ile |
S114 |
22 | BAA03g45450 | A03 | 21748449 | G | A | synonymous_variant | LOW | c.2007C>T|p.Asp669Asp |
S185 |
23 | BAA03g45450 | A03 | 21748482 | C | T | stop_gained | HIGH | c.1974G>A|p.Trp658* |
S273 |
24 | BAA03g45450 | A03 | 21750657 | C | T | intron_variant | MODIFIER | c.329+116G>A| |
S131 |
25 | BAA03g45450 | A03 | 21751691 | C | T | upstream_gene_variant | MODIFIER | c.-590G>A| |
S172 S217 |