Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26760 | A10 | 21088750 | C | T | splice_region_variant&stop_retained_variant | LOW | c.1568G>A|p.Ter523Ter |
S103 |
2 | BAA10g26760 | A10 | 21089152 | C | T | missense_variant | MODERATE | c.1357G>A|p.Asp453Asn |
S246 |
3 | BAA10g26760 | A10 | 21090017 | C | T | stop_gained | HIGH | c.753G>A|p.Trp251* |
S5 |
4 | BAA10g26760 | A10 | 21090575 | G | A | synonymous_variant | LOW | c.195C>T|p.Ser65Ser |
S125 |
5 | BAA10g26760 | A10 | 21090589 | C | T | missense_variant | MODERATE | c.181G>A|p.Glu61Lys |
S275 |
6 | BAA10g26760 | A10 | 21091828 | C | T | upstream_gene_variant | MODIFIER | c.-1059G>A| |
S33 |
7 | BAA10g26760 | A10 | 21091886 | G | A | upstream_gene_variant | MODIFIER | c.-1117C>T| |
S144 S240 |