Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07420 | A10 | 4264249 | C | T | missense_variant | MODERATE | c.2344G>A|p.Glu782Lys |
S104 S52 |
2 | BAA10g07420 | A10 | 4264268 | C | T | synonymous_variant | LOW | c.2325G>A|p.Glu775Glu |
S113 |
3 | BAA10g07420 | A10 | 4265161 | C | T | stop_gained | HIGH | c.1965G>A|p.Trp655* |
S115 |
4 | BAA10g07420 | A10 | 4265799 | C | T | missense_variant | MODERATE | c.1657G>A|p.Glu553Lys |
S56 |
5 | BAA10g07420 | A10 | 4265848 | G | A | intron_variant | MODIFIER | c.1627-19C>T| |
S99 |
6 | BAA10g07420 | A10 | 4266128 | C | T | missense_variant | MODERATE | c.1481G>A|p.Arg494Gln |
S159 S243 S299 |
7 | BAA10g07420 | A10 | 4266749 | C | T | missense_variant&splice_region_variant | MODERATE | c.1312G>A|p.Glu438Lys |
S89 |
8 | BAA10g07420 | A10 | 4267166 | C | T | missense_variant | MODERATE | c.1156G>A|p.Glu386Lys |
S287 |
9 | BAA10g07420 | A10 | 4270698 | C | T | missense_variant | MODERATE | c.121G>A|p.Val41Ile |
S269 |
10 | BAA10g07420 | A10 | 4272035 | C | T | upstream_gene_variant | MODIFIER | c.-1071G>A| |
S272 |
11 | BAA10g07420 | A10 | 4272965 | T | C | upstream_gene_variant | MODIFIER | c.-2001A>G| |
S10 S108 S120 S125 S15 S164 S169 S19 S200 S260 S279 S284 S298 S30 S35 S4 S6 S62 S83 |
12 | BAA10g07420 | A10 | 4273212 | G | A | upstream_gene_variant | MODIFIER | c.-2248C>T| |
S237 |
13 | BAA10g07420 | A10 | 4273500 | T | G | upstream_gene_variant | MODIFIER | c.-2536A>C| |
S288 |
14 | BAA10g07420 | A10 | 4275437 | C | T | upstream_gene_variant | MODIFIER | c.-4473G>A| |
S287 |