Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04300 | A10 | 2160679 | C | T | missense_variant | MODERATE | c.1510G>A|p.Asp504Asn |
S89 |
2 | BAA10g04300 | A10 | 2160711 | C | T | stop_gained | HIGH | c.1478G>A|p.Trp493* |
S135 |
3 | BAA10g04300 | A10 | 2160900 | C | T | missense_variant&splice_region_variant | MODERATE | c.1453G>A|p.Ala485Thr |
S281 |
4 | BAA10g04300 | A10 | 2161024 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1330-1G>A| |
S246 |
5 | BAA10g04300 | A10 | 2162279 | G | A | synonymous_variant | LOW | c.1326C>T|p.Leu442Leu |
S53 |
6 | BAA10g04300 | A10 | 2162565 | C | T | missense_variant | MODERATE | c.1129G>A|p.Glu377Lys |
S44 |
7 | BAA10g04300 | A10 | 2162718 | C | T | missense_variant | MODERATE | c.976G>A|p.Glu326Lys |
S114 |
8 | BAA10g04300 | A10 | 2162787 | C | T | missense_variant | MODERATE | c.907G>A|p.Glu303Lys |
S146 |
9 | BAA10g04300 | A10 | 2162842 | C | T | synonymous_variant | LOW | c.852G>A|p.Gly284Gly |
S287 |
10 | BAA10g04300 | A10 | 2162870 | C | T | missense_variant | MODERATE | c.824G>A|p.Arg275His |
S294 |
11 | BAA10g04300 | A10 | 2165072 | G | A | synonymous_variant | LOW | c.213C>T|p.Leu71Leu |
S282 |
12 | BAA10g04300 | A10 | 2166903 | C | T | missense_variant | MODERATE | c.47G>A|p.Gly16Glu |
S120 |
13 | BAA10g04300 | A10 | 2167793 | C | T | upstream_gene_variant | MODIFIER | c.-844G>A| |
S297 |
14 | BAA10g04300 | A10 | 2168883 | G | A | upstream_gene_variant | MODIFIER | c.-1934C>T| |
S161 |
15 | BAA10g04300 | A10 | 2169960 | C | T | upstream_gene_variant | MODIFIER | c.-3011G>A| |
S265 |
16 | BAA10g04300 | A10 | 2170106 | C | T | upstream_gene_variant | MODIFIER | c.-3157G>A| |
S297 |
17 | BAA10g04300 | A10 | 2170946 | C | T | upstream_gene_variant | MODIFIER | c.-3997G>A| |
S195 |