Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18990 | A10 | 17584660 | G | A | missense_variant | MODERATE | c.1108C>T|p.Pro370Ser |
S167 |
2 | BAA10g18990 | A10 | 17584702 | G | A | missense_variant | MODERATE | c.1066C>T|p.Arg356Cys |
S233 |
3 | BAA10g18990 | A10 | 17584763 | G | A | synonymous_variant | LOW | c.1005C>T|p.Tyr335Tyr |
S63 |
4 | BAA10g18990 | A10 | 17586053 | C | T | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S60 |
5 | BAA10g18990 | A10 | 17586069 | C | T | synonymous_variant | LOW | c.213G>A|p.Arg71Arg |
S269 |
6 | BAA10g18990 | A10 | 17588115 | G | A | upstream_gene_variant | MODIFIER | c.-714C>T| |
S295 |
7 | BAA10g18990 | A10 | 17588634 | C | T | upstream_gene_variant | MODIFIER | c.-1233G>A| |
S202 |
8 | BAA10g18990 | A10 | 17589597 | C | T | upstream_gene_variant | MODIFIER | c.-2196G>A| |
S119 |
9 | BAA10g18990 | A10 | 17589681 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S108 |
10 | BAA10g18990 | A10 | 17589748 | C | T | upstream_gene_variant | MODIFIER | c.-2347G>A| |
S160 |
11 | BAA10g18990 | A10 | 17590334 | C | T | upstream_gene_variant | MODIFIER | c.-2933G>A| |
S2 |
12 | BAA10g18990 | A10 | 17590653 | G | A | upstream_gene_variant | MODIFIER | c.-3252C>T| |
S180 |
13 | BAA10g18990 | A10 | 17590865 | A | C | upstream_gene_variant | MODIFIER | c.-3464T>G| |
S54 |
14 | BAA10g18990 | A10 | 17592117 | C | T | upstream_gene_variant | MODIFIER | c.-4716G>A| |
S146 |
15 | BAA10g18990 | A10 | 17592277 | C | T | upstream_gene_variant | MODIFIER | c.-4876G>A| |
S10 |