Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42740 | A05 | 40353865 | C | T | upstream_gene_variant | MODIFIER | c.-3833C>T| |
S260 |
2 | BAA05g42740 | A05 | 40354523 | C | T | upstream_gene_variant | MODIFIER | c.-3175C>T| |
S270 |
3 | BAA05g42740 | A05 | 40355091 | C | T | upstream_gene_variant | MODIFIER | c.-2607C>T| |
S15 S3 |
4 | BAA05g42740 | A05 | 40355435 | G | A | upstream_gene_variant | MODIFIER | c.-2263G>A| |
S130 |
5 | BAA05g42740 | A05 | 40356105 | C | T | upstream_gene_variant | MODIFIER | c.-1593C>T| |
S90 |
6 | BAA05g42740 | A05 | 40357536 | C | T | upstream_gene_variant | MODIFIER | c.-162C>T| |
S207 |
7 | BAA05g42740 | A05 | 40357778 | G | A | synonymous_variant | LOW | c.81G>A|p.Thr27Thr |
S174 |
8 | BAA05g42740 | A05 | 40357813 | C | T | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S162 |
9 | BAA05g42740 | A05 | 40358643 | G | A | intron_variant | MODIFIER | c.211-50G>A| |
S61 |
10 | BAA05g42740 | A05 | 40358933 | G | A | missense_variant | MODERATE | c.451G>A|p.Ala151Thr |
S287 |
11 | BAA05g42740 | A05 | 40359168 | G | A | missense_variant | MODERATE | c.686G>A|p.Arg229Gln |
S17 |
12 | BAA05g42740 | A05 | 40359335 | G | A | missense_variant | MODERATE | c.853G>A|p.Asp285Asn |
S159 |
13 | BAA05g42740 | A05 | 40359378 | G | A | missense_variant | MODERATE | c.896G>A|p.Gly299Glu |
S133 |
14 | BAA05g42740 | A05 | 40360397 | C | T | missense_variant | MODERATE | c.1595C>T|p.Pro532Leu |
S165 |
15 | BAA05g42740 | A05 | 40360487 | C | T | missense_variant | MODERATE | c.1685C>T|p.Ser562Leu |
S45 |
16 | BAA05g42740 | A05 | 40361042 | G | A | missense_variant | MODERATE | c.2240G>A|p.Arg747Lys |
S12 |
17 | BAA05g42740 | A05 | 40362552 | C | T | missense_variant | MODERATE | c.3169C>T|p.Leu1057Phe |
S305 |
18 | BAA05g42740 | A05 | 40362931 | G | A | missense_variant | MODERATE | c.3548G>A|p.Cys1183Tyr |
S249 |
19 | BAA05g42740 | A05 | 40362932 | C | T | synonymous_variant | LOW | c.3549C>T|p.Cys1183Cys |
S262 |