Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44230 | A09 | 50007100 | G | A | missense_variant | MODERATE | c.2888C>T|p.Thr963Ile |
S162 |
2 | BAA09g44230 | A09 | 50007218 | G | A | missense_variant | MODERATE | c.2770C>T|p.His924Tyr |
S288 |
3 | BAA09g44230 | A09 | 50008214 | C | T | missense_variant | MODERATE | c.1939G>A|p.Asp647Asn |
S191 |
4 | BAA09g44230 | A09 | 50008519 | C | T | missense_variant | MODERATE | c.1729G>A|p.Val577Ile |
S183 S198 |
5 | BAA09g44230 | A09 | 50008868 | C | T | synonymous_variant | LOW | c.1380G>A|p.Pro460Pro |
S174 |
6 | BAA09g44230 | A09 | 50010088 | C | T | missense_variant | MODERATE | c.346G>A|p.Ala116Thr |
S14 |
7 | BAA09g44230 | A09 | 50010190 | C | T | missense_variant | MODERATE | c.244G>A|p.Glu82Lys |
S30 S31 |
8 | BAA09g44230 | A09 | 50010762 | C | T | upstream_gene_variant | MODIFIER | c.-329G>A| |
S5 |
9 | BAA09g44230 | A09 | 50011545 | G | A | upstream_gene_variant | MODIFIER | c.-1112C>T| |
S47 |
10 | BAA09g44230 | A09 | 50011978 | G | A | upstream_gene_variant | MODIFIER | c.-1545C>T| |
S308 |
11 | BAA09g44230 | A09 | 50012209 | G | A | upstream_gene_variant | MODIFIER | c.-1776C>T| |
S246 |
12 | BAA09g44230 | A09 | 50012637 | G | A | upstream_gene_variant | MODIFIER | c.-2204C>T| |
S202 |
13 | BAA09g44230 | A09 | 50015353 | T | A | upstream_gene_variant | MODIFIER | c.-4920A>T| |
S183 S198 |