| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.72007707C>A | CA377145785 | CHST3 | c.676C>A (p.Arg226Ser) | |
| 10 | g.72007707C= | CA1918976152 | CHST3 | c.676C= (p.Arg226=) | |
| 10 | g.72007707C>G | CA377145787 | CHST3 | c.676C>G (p.Arg226Gly) | gnomAD v4 |
| 10 | g.72007707C>T | CA377145779 | CHST3 | c.676C>T (p.Arg226Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.72007708G>A | CA377145791 | CHST3 | c.677G>A (p.Arg226His) | gnomAD v4 |
| 10 | g.72007708G>C | CA377145793 | CHST3 | c.677G>C (p.Arg226Pro) | |
| 10 | g.72007708G= | CA1918976154 | CHST3 | c.677G= (p.Arg226=) | |
| 10 | g.72007708G>T | CA377145794 | CHST3 | c.677G>T (p.Arg226Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.72007709C>A | CA470283774 | CHST3 | c.678C>A (p.Arg226=) | |
| 10 | g.72007709C>G | CA470283773 | CHST3 | c.678C>G (p.Arg226=) | |
| 10 | g.72007709C>T | CA470283772 | CHST3 | c.678C>T (p.Arg226=) | |
| 10 | g.72007710T>A | CA377145795 | CHST3 | c.679T>A (p.Ser227Thr) | |
| 10 | g.72007710T>C | CA377145796 | CHST3 | c.679T>C (p.Ser227Pro) | |
| 10 | g.72007710T>G | CA377145799 | CHST3 | c.679T>G (p.Ser227Ala) | gnomAD v4 |
| 10 | g.72007711C>A | CA377145809 | CHST3 | c.680C>A (p.Ser227Tyr) | gnomAD v4 |
| 10 | g.72007711C= | CA1918976159 | CHST3 | c.680C= (p.Ser227=) | |
| 10 | g.72007711C>G | CA377145805 | CHST3 | c.680C>G (p.Ser227Cys) | ClinVar dbSNP gnomAD v4 |
| 10 | g.72007711C>T | CA377145807 | CHST3 | c.680C>T (p.Ser227Phe) | gnomAD v4 |
| 10 | g.72007712C>A | CA470283776 | CHST3 | c.681C>A (p.Ser227=) | gnomAD v4 |
| 10 | g.72007712C= | CA1918976164 | CHST3 | c.681C= (p.Ser227=) | |
| 10 | g.72007712C>G | CA470283777 | CHST3 | c.681C>G (p.Ser227=) | ClinVar dbSNP |
| 10 | g.72007712C>T | CA470283779 | CHST3 | c.681C>T (p.Ser227=) | dbSNP gnomAD v4 |
| 10 | g.72007713C>A | CA377145812 | CHST3 | c.682C>A (p.Leu228Met) | gnomAD v4 |
| 10 | g.72007713C>G | CA377145842 | CHST3 | c.682C>G (p.Leu228Val) | |
| 10 | g.72007713C>T | CA470283780 | CHST3 | c.682C>T (p.Leu228=) | gnomAD v4 |
| 10 | g.72007714T>A | CA377145852 | CHST3 | c.683T>A (p.Leu228Gln) | |
| 10 | g.72007714T>C | CA377145859 | CHST3 | c.683T>C (p.Leu228Pro) | |
| 10 | g.72007714T>G | CA377145861 | CHST3 | c.683T>G (p.Leu228Arg) | |
| 10 | g.72007715G>A | CA470283781 | CHST3 | c.684G>A (p.Leu228=) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.72007715G>C | CA470283783 | CHST3 | c.684G>C (p.Leu228=) | |
| 10 | g.72007715G= | CA1918976167 | CHST3 | c.684G= (p.Leu228=) | |
| 10 | g.72007715G>T | CA470283782 | CHST3 | c.684G>T (p.Leu228=) | gnomAD v4 |
| 10 | g.72007716T>A | CA377145864 | CHST3 | c.685T>A (p.Cys229Ser) | |
| 10 | g.72007716T>C | CA377145866 | CHST3 | c.685T>C (p.Cys229Arg) | |
| 10 | g.72007716T>G | CA377145865 | CHST3 | c.685T>G (p.Cys229Gly) | |
| 10 | g.72007717G>A | CA377145870 | CHST3 | c.686G>A (p.Cys229Tyr) | dbSNP gnomAD v4 |
| 10 | g.72007717G>C | CA377145878 | CHST3 | c.686G>C (p.Cys229Ser) | |
| 10 | g.72007717G= | CA1918976170 | CHST3 | c.686G= (p.Cys229=) | |
| 10 | g.72007717G>T | CA377145880 | CHST3 | c.686G>T (p.Cys229Phe) | gnomAD v4 |
| 10 | g.72007718C>A | CA377145885 | CHST3 | c.687C>A (p.Cys229Ter) | gnomAD v4 |
| 10 | g.72007718C= | CA1918976172 | CHST3 | c.687C= (p.Cys229=) | |
| 10 | g.72007718C>G | CA377145889 | CHST3 | c.687C>G (p.Cys229Trp) | |
| 10 | g.72007718C>T | CA470283784 | CHST3 | c.687C>T (p.Cys229=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.72007719G>A | CA5548147 | CHST3 | c.688G>A (p.Glu230Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.72007719G>C | CA377145892 | CHST3 | c.688G>C (p.Glu230Gln) | |
| 10 | g.72007719G= | CA1918976176 | CHST3 | c.688G= (p.Glu230=) | |
| 10 | g.72007719G>T | CA377145893 | CHST3 | c.688G>T (p.Glu230Ter) | ClinVar dbSNP gnomAD v4 |
| 10 | g.72007720A>C | CA377145899 | CHST3 | c.689A>C (p.Glu230Ala) | |
| 10 | g.72007720A>G | CA377145900 | CHST3 | c.689A>G (p.Glu230Gly) | |
| 10 | g.72007720A>T | CA377145901 | CHST3 | c.689A>T (p.Glu230Val) | COSMIC |