Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16540 | A05 | 9172620 | G | A | upstream_gene_variant | MODIFIER | c.-3159G>A| |
S139 |
2 | BAA05g16540 | A05 | 9174535 | C | T | upstream_gene_variant | MODIFIER | c.-1244C>T| |
S237 |
3 | BAA05g16540 | A05 | 9175581 | G | A | upstream_gene_variant | MODIFIER | c.-198G>A| |
S192 |
4 | BAA05g16540 | A05 | 9175893 | G | A | missense_variant | MODERATE | c.115G>A|p.Glu39Lys |
S260 |
5 | BAA05g16540 | A05 | 9175909 | C | T | missense_variant | MODERATE | c.131C>T|p.Ser44Leu |
S268 |
6 | BAA05g16540 | A05 | 9176052 | C | T | missense_variant | MODERATE | c.274C>T|p.Pro92Ser |
S143 |
7 | BAA05g16540 | A05 | 9176484 | G | A | missense_variant | MODERATE | c.706G>A|p.Asp236Asn |
S13 S168 S219 S64 S72 |
8 | BAA05g16540 | A05 | 9176961 | C | T | stop_gained | HIGH | c.1183C>T|p.Gln395* |
S292 |
9 | BAA05g16540 | A05 | 9177033 | C | T | missense_variant | MODERATE | c.1255C>T|p.Pro419Ser |
S143 |
10 | BAA05g16540 | A05 | 9177179 | C | T | synonymous_variant | LOW | c.1401C>T|p.His467His |
S164 |
11 | BAA05g16540 | A05 | 9177670 | G | A | missense_variant | MODERATE | c.1892G>A|p.Gly631Asp |
S217 |
12 | BAA05g16540 | A05 | 9177966 | G | A | missense_variant | MODERATE | c.2188G>A|p.Asp730Asn |
S32 |
13 | BAA05g16540 | A05 | 9178297 | C | T | missense_variant | MODERATE | c.2353C>T|p.Pro785Ser |
S181 |
14 | BAA05g16540 | A05 | 9178578 | G | A | intron_variant | MODIFIER | c.2360-96G>A| |
S172 |
15 | BAA05g16540 | A05 | 9179831 | G | A | intron_variant | MODIFIER | c.3490+27G>A| |
S218 |
16 | BAA05g16540 | A05 | 9180301 | C | T | stop_gained | HIGH | c.3796C>T|p.Gln1266* |
S286 |
17 | BAA05g16540 | A05 | 9180846 | G | A | missense_variant | MODERATE | c.4262G>A|p.Arg1421Lys |
S4 |
18 | BAA05g16540 | A05 | 9183062 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.5710-1G>A| |
S7 |
19 | BAA05g16540 | A05 | 9184821 | C | T | missense_variant | MODERATE | c.6422C>T|p.Thr2141Ile |
S69 |
20 | BAA05g16540 | A05 | 9184874 | G | A | missense_variant | MODERATE | c.6475G>A|p.Glu2159Lys |
S174 S27 S39 |
21 | BAA05g16540 | A05 | 9186659 | C | T | missense_variant | MODERATE | c.6958C>T|p.Pro2320Ser |
S27 |
22 | BAA05g16540 | A05 | 9187226 | G | A | downstream_gene_variant | MODIFIER | c.*228G>A| |
S100 |