Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12180 | A01 | 5712324 | C | T | missense_variant | MODERATE | c.7007G>A|p.Arg2336Gln |
S221 |
2 | BAA01g12180 | A01 | 5713231 | C | T | missense_variant | MODERATE | c.6361G>A|p.Asp2121Asn |
S120 |
3 | BAA01g12180 | A01 | 5714200 | C | T | synonymous_variant | LOW | c.5628G>A|p.Arg1876Arg |
S128 |
4 | BAA01g12180 | A01 | 5714830 | G | A | missense_variant | MODERATE | c.5216C>T|p.Ser1739Phe |
S12 |
5 | BAA01g12180 | A01 | 5714989 | G | A | missense_variant | MODERATE | c.5144C>T|p.Thr1715Ile |
S188 |
6 | BAA01g12180 | A01 | 5716058 | A | T | intron_variant | MODIFIER | c.4306-105T>A| |
S95 |
7 | BAA01g12180 | A01 | 5716458 | C | T | missense_variant | MODERATE | c.4046G>A|p.Gly1349Asp |
S277 |
8 | BAA01g12180 | A01 | 5716471 | G | A | missense_variant | MODERATE | c.4033C>T|p.Pro1345Ser |
S193 |
9 | BAA01g12180 | A01 | 5716593 | G | A | missense_variant | MODERATE | c.4001C>T|p.Pro1334Leu |
S240 |
10 | BAA01g12180 | A01 | 5717250 | C | T | stop_gained | HIGH | c.3539G>A|p.Trp1180* |
S202 |
11 | BAA01g12180 | A01 | 5717557 | C | T | synonymous_variant | LOW | c.3315G>A|p.Glu1105Glu |
S223 |
12 | BAA01g12180 | A01 | 5717966 | C | T | missense_variant | MODERATE | c.2981G>A|p.Gly994Glu |
S278 |
13 | BAA01g12180 | A01 | 5718326 | C | T | missense_variant | MODERATE | c.2714G>A|p.Arg905Gln |
S50 |
14 | BAA01g12180 | A01 | 5720209 | C | T | synonymous_variant | LOW | c.1143G>A|p.Pro381Pro |
S99 |
15 | BAA01g12180 | A01 | 5722233 | G | A | upstream_gene_variant | MODIFIER | c.-559C>T| |
S174 |