Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27380 | A10 | 21378248 | G | A | missense_variant | MODERATE | c.2144C>T|p.Pro715Leu |
S251 |
2 | BAA10g27380 | A10 | 21378465 | G | A | synonymous_variant | LOW | c.2046C>T|p.Asn682Asn |
S216 |
3 | BAA10g27380 | A10 | 21378689 | C | T | missense_variant | MODERATE | c.1936G>A|p.Glu646Lys |
S119 |
4 | BAA10g27380 | A10 | 21378902 | G | A | synonymous_variant | LOW | c.1723C>T|p.Leu575Leu |
S178 |
5 | BAA10g27380 | A10 | 21379870 | G | A | missense_variant | MODERATE | c.1079C>T|p.Ser360Phe |
S293 |
6 | BAA10g27380 | A10 | 21380336 | C | T | missense_variant&splice_region_variant | MODERATE | c.968G>A|p.Ser323Asn |
S162 |
7 | BAA10g27380 | A10 | 21381758 | C | T | missense_variant | MODERATE | c.109G>A|p.Gly37Ser |
S302 |
8 | BAA10g27380 | A10 | 21382893 | G | A | upstream_gene_variant | MODIFIER | c.-942C>T| |
S99 |
9 | BAA10g27380 | A10 | 21383011 | G | A | upstream_gene_variant | MODIFIER | c.-1060C>T| |
S190 |
10 | BAA10g27380 | A10 | 21384154 | G | A | upstream_gene_variant | MODIFIER | c.-2203C>T| |
S193 |
11 | BAA10g27380 | A10 | 21384169 | C | T | upstream_gene_variant | MODIFIER | c.-2218G>A| |
S144 |
12 | BAA10g27380 | A10 | 21384206 | G | A | upstream_gene_variant | MODIFIER | c.-2255C>T| |
S88 |
13 | BAA10g27380 | A10 | 21386607 | C | T | upstream_gene_variant | MODIFIER | c.-4656G>A| |
S204 |
14 | BAA10g27380 | A10 | 21386614 | G | A | upstream_gene_variant | MODIFIER | c.-4663C>T| |
S278 |