Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20790 | A10 | 18539034 | C | T | missense_variant | MODERATE | c.1994G>A|p.Gly665Glu |
S155 |
2 | BAA10g20790 | A10 | 18539344 | C | T | missense_variant | MODERATE | c.1765G>A|p.Asp589Asn |
S286 |
3 | BAA10g20790 | A10 | 18539363 | C | T | splice_region_variant&intron_variant | LOW | c.1750-4G>A| |
S113 |
4 | BAA10g20790 | A10 | 18539473 | C | T | missense_variant | MODERATE | c.1741G>A|p.Asp581Asn |
S95 |
5 | BAA10g20790 | A10 | 18540726 | C | T | splice_region_variant&intron_variant | LOW | c.1034+8G>A| |
S266 |
6 | BAA10g20790 | A10 | 18543244 | G | A | synonymous_variant | LOW | c.216C>T|p.Tyr72Tyr |
S174 S241 |
7 | BAA10g20790 | A10 | 18543792 | G | A | synonymous_variant | LOW | c.123C>T|p.Leu41Leu |
S233 |
8 | BAA10g20790 | A10 | 18544239 | G | A | upstream_gene_variant | MODIFIER | c.-325C>T| |
S159 S243 |
9 | BAA10g20790 | A10 | 18544975 | C | T | upstream_gene_variant | MODIFIER | c.-1061G>A| |
S183 |
10 | BAA10g20790 | A10 | 18545013 | G | A | upstream_gene_variant | MODIFIER | c.-1099C>T| |
S264 |
11 | BAA10g20790 | A10 | 18546186 | C | T | upstream_gene_variant | MODIFIER | c.-2272G>A| |
S18 |
12 | BAA10g20790 | A10 | 18546793 | G | A | upstream_gene_variant | MODIFIER | c.-2879C>T| |
S159 S243 |