Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11570 | A08 | 10226081 | C | T | missense_variant | MODERATE | c.3875G>A|p.Arg1292Lys |
S160 |
2 | BAA08g11570 | A08 | 10226443 | T | C | missense_variant | MODERATE | c.3653A>G|p.Glu1218Gly |
S186 |
3 | BAA08g11570 | A08 | 10227070 | C | T | missense_variant | MODERATE | c.3289G>A|p.Glu1097Lys |
S178 |
4 | BAA08g11570 | A08 | 10227199 | C | T | missense_variant | MODERATE | c.3160G>A|p.Asp1054Asn |
S173 |
5 | BAA08g11570 | A08 | 10227676 | C | T | missense_variant | MODERATE | c.2683G>A|p.Asp895Asn |
S216 |
6 | BAA08g11570 | A08 | 10227762 | C | T | missense_variant | MODERATE | c.2597G>A|p.Gly866Glu |
S36 |
7 | BAA08g11570 | A08 | 10229085 | G | A | missense_variant | MODERATE | c.1274C>T|p.Ser425Phe |
S98 |
8 | BAA08g11570 | A08 | 10229097 | G | A | missense_variant | MODERATE | c.1262C>T|p.Ser421Phe |
S288 |
9 | BAA08g11570 | A08 | 10229468 | C | T | stop_gained | HIGH | c.1037G>A|p.Trp346* |
S36 |
10 | BAA08g11570 | A08 | 10229931 | A | C | synonymous_variant | LOW | c.942T>G|p.Val314Val |
S177 S286 |
11 | BAA08g11570 | A08 | 10230879 | C | T | upstream_gene_variant | MODIFIER | c.-7G>A| |
S148 S30 S31 |
12 | BAA08g11570 | A08 | 10230974 | C | T | upstream_gene_variant | MODIFIER | c.-102G>A| |
S55 |
13 | BAA08g11570 | A08 | 10235389 | C | T | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S157 S163 |