Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49020 | A09 | 52590477 | G | A | missense_variant | MODERATE | c.1745C>T|p.Ser582Phe |
S184 |
2 | BAA09g49020 | A09 | 52590736 | C | T | missense_variant | MODERATE | c.1486G>A|p.Asp496Asn |
S103 |
3 | BAA09g49020 | A09 | 52591310 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.989-1G>A| |
S140 |
4 | BAA09g49020 | A09 | 52591915 | G | A | synonymous_variant | LOW | c.654C>T|p.Val218Val |
S175 S177 |
5 | BAA09g49020 | A09 | 52591977 | C | T | missense_variant | MODERATE | c.592G>A|p.Glu198Lys |
S297 |
6 | BAA09g49020 | A09 | 52592511 | C | T | missense_variant&splice_region_variant | MODERATE | c.247G>A|p.Val83Met |
S33 |
7 | BAA09g49020 | A09 | 52592632 | G | A | synonymous_variant | LOW | c.201C>T|p.Ile67Ile |
S308 |
8 | BAA09g49020 | A09 | 52592652 | C | T | missense_variant | MODERATE | c.181G>A|p.Asp61Asn |
S9 |
9 | BAA09g49020 | A09 | 52594084 | G | A | upstream_gene_variant | MODIFIER | c.-1252C>T| |
S283 |
10 | BAA09g49020 | A09 | 52594203 | G | A | upstream_gene_variant | MODIFIER | c.-1371C>T| |
S161 |
11 | BAA09g49020 | A09 | 52594223 | G | A | upstream_gene_variant | MODIFIER | c.-1391C>T| |
S185 |
12 | BAA09g49020 | A09 | 52594663 | C | T | upstream_gene_variant | MODIFIER | c.-1831G>A| |
S61 |
13 | BAA09g49020 | A09 | 52594807 | C | T | upstream_gene_variant | MODIFIER | c.-1975G>A| |
S18 |
14 | BAA09g49020 | A09 | 52596617 | C | T | upstream_gene_variant | MODIFIER | c.-3785G>A| |
S96 |
15 | BAA09g49020 | A09 | 52597077 | G | A | upstream_gene_variant | MODIFIER | c.-4245C>T| |
S59 |