Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19530 | A10 | 17875353 | C | T | downstream_gene_variant | MODIFIER | c.*4441G>A| |
S209 |
2 | BAA10g19530 | A10 | 17875362 | G | A | downstream_gene_variant | MODIFIER | c.*4432C>T| |
S142 |
3 | BAA10g19530 | A10 | 17875410 | G | A | downstream_gene_variant | MODIFIER | c.*4384C>T| |
S142 |
4 | BAA10g19530 | A10 | 17875789 | G | A | downstream_gene_variant | MODIFIER | c.*4005C>T| |
S162 |
5 | BAA10g19530 | A10 | 17875805 | G | A | downstream_gene_variant | MODIFIER | c.*3989C>T| |
S61 |
6 | BAA10g19530 | A10 | 17875926 | C | T | downstream_gene_variant | MODIFIER | c.*3868G>A| |
S38 |
7 | BAA10g19530 | A10 | 17875987 | C | T | downstream_gene_variant | MODIFIER | c.*3807G>A| |
S166 |
8 | BAA10g19530 | A10 | 17876272 | G | A | downstream_gene_variant | MODIFIER | c.*3522C>T| |
S197 |
9 | BAA10g19530 | A10 | 17876375 | C | T | downstream_gene_variant | MODIFIER | c.*3419G>A| |
S199 |
10 | BAA10g19530 | A10 | 17880994 | C | T | missense_variant | MODERATE | c.1034G>A|p.Arg345Lys |
S305 |
11 | BAA10g19530 | A10 | 17882141 | C | T | missense_variant | MODERATE | c.695G>A|p.Arg232Lys |
S67 |
12 | BAA10g19530 | A10 | 17882371 | G | A | synonymous_variant | LOW | c.465C>T|p.Tyr155Tyr |
S61 |
13 | BAA10g19530 | A10 | 17882584 | G | A | synonymous_variant | LOW | c.252C>T|p.Ser84Ser |
S65 |
14 | BAA10g19530 | A10 | 17883185 | G | A | upstream_gene_variant | MODIFIER | c.-350C>T| |
S184 |
15 | BAA10g19530 | A10 | 17884228 | G | A | upstream_gene_variant | MODIFIER | c.-1393C>T| |
S178 |
16 | BAA10g19530 | A10 | 17886408 | C | T | upstream_gene_variant | MODIFIER | c.-3573G>A| |
S37 |
17 | BAA10g19530 | A10 | 17886645 | G | A | upstream_gene_variant | MODIFIER | c.-3810C>T| |
S71 |
18 | BAA10g19530 | A10 | 17886974 | G | A | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S255 |