| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.48728342_48728343delinsTC | CA2263242612 | HOXB13 | c.251_252delinsGA (p.Gly84=) | |
| 17 | g.48728343C>A | CA400107834 | HOXB13 | c.251G>T (p.Gly84Val) | |
| 17 | g.48728343C= | CA2263242613 | HOXB13 | c.251G= (p.Gly84=) | |
| 17 | g.48728343C>G | CA400107835 | HOXB13 | c.251G>C (p.Gly84Ala) | |
| 17 | g.48728343C>T | CA288225 | HOXB13 | c.251G>A (p.Gly84Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.48728344del | CA915950441 | HOXB13 | c.251del (p.Gly84GlufsTer14) | ClinVar dbSNP |
| 17 | g.48728344C>A | CA400107838 | HOXB13 | c.250G>T (p.Gly84Ter) | |
| 17 | g.48728344C>G | CA400107836 | HOXB13 | c.250G>C (p.Gly84Arg) | |
| 17 | g.48728344C>T | CA400107837 | HOXB13 | c.250G>A (p.Gly84Arg) | gnomAD v4 |
| 17 | g.48728344_48728345delinsCA | CA2263242614 | HOXB13 | c.249_250delinsTG (p.Phe83=) | |
| 17 | g.48728345A>C | CA400107839 | HOXB13 | c.249T>G (p.Phe83Leu) | |
| 17 | g.48728345A>G | CA500661991 | HOXB13 | c.249T>C (p.Phe83=) | |
| 17 | g.48728345A>T | CA400107840 | HOXB13 | c.249T>A (p.Phe83Leu) | |
| 17 | g.48728347del | CA915950442 | HOXB13 | c.249del (p.Phe83LeufsTer15) | ClinVar dbSNP |
| 17 | g.48728346A= | CA2263242615 | HOXB13 | c.248T= (p.Phe83=) | |
| 17 | g.48728346A>C | CA400107841 | HOXB13 | c.248T>G (p.Phe83Cys) | |
| 17 | g.48728346A>G | CA400107842 | HOXB13 | c.248T>C (p.Phe83Ser) | ClinVar dbSNP |
| 17 | g.48728346A>T | CA400107843 | HOXB13 | c.248T>A (p.Phe83Tyr) | |
| 17 | g.48728347A>C | CA400107844 | HOXB13 | c.247T>G (p.Phe83Val) | |
| 17 | g.48728347A>G | CA400107846 | HOXB13 | c.247T>C (p.Phe83Leu) | |
| 17 | g.48728347A>T | CA400107845 | HOXB13 | c.247T>A (p.Phe83Ile) | ClinVar |
| 17 | g.48728348G>A | CA500661992 | HOXB13 | c.246C>T (p.Tyr82=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.48728348G>C | CA400107847 | HOXB13 | c.246C>G (p.Tyr82Ter) | |
| 17 | g.48728348G= | CA2263242616 | HOXB13 | c.246C= (p.Tyr82=) | |
| 17 | g.48728348G>T | CA400107848 | HOXB13 | c.246C>A (p.Tyr82Ter) | |
| 17 | g.48728349T>A | CA400107849 | HOXB13 | c.245A>T (p.Tyr82Phe) | |
| 17 | g.48728349T>C | CA400107850 | HOXB13 | c.245A>G (p.Tyr82Cys) | |
| 17 | g.48728349T>G | CA400107851 | HOXB13 | c.245A>C (p.Tyr82Ser) | ClinVar dbSNP gnomAD v4 |
| 17 | g.48728349T= | CA2263242617 | HOXB13 | c.245A= (p.Tyr82=) | |
| 17 | g.48728350A= | CA2263242619 | HOXB13 | c.244T= (p.Tyr82=) | |
| 17 | g.48728350A>C | CA400107852 | HOXB13 | c.244T>G (p.Tyr82Asp) | ClinVar dbSNP |
| 17 | g.48728350A>G | CA400107853 | HOXB13 | c.244T>C (p.Tyr82His) | gnomAD v4 |
| 17 | g.48728350A>T | CA400107854 | HOXB13 | c.244T>A (p.Tyr82Asn) | ClinVar dbSNP |
| 17 | g.48728351dup | CA2263242618 | HOXB13 | c.244dup (p.Tyr82LeufsTer?) | ClinVar dbSNP |
| 17 | g.48728351A>C | CA500661993 | HOXB13 | c.243T>G (p.Gly81=) | |
| 17 | g.48728351A>G | CA500661994 | HOXB13 | c.243T>C (p.Gly81=) | ClinVar dbSNP |
| 17 | g.48728351A>T | CA500661995 | HOXB13 | c.243T>A (p.Gly81=) | |
| 17 | g.48728352C>A | CA400107855 | HOXB13 | c.242G>T (p.Gly81Val) | ClinVar dbSNP |
| 17 | g.48728352C= | CA2263242620 | HOXB13 | c.242G= (p.Gly81=) | |
| 17 | g.48728352C>G | CA400107856 | HOXB13 | c.242G>C (p.Gly81Ala) | |
| 17 | g.48728352C>T | CA400107857 | HOXB13 | c.242G>A (p.Gly81Asp) | ClinVar dbSNP |
| 17 | g.48728353del | CA2733710640 | HOXB13 | c.242del (p.Gly81ValfsTer17) | dbSNP |
| 17 | g.48728353C>A | CA400107858 | HOXB13 | c.241G>T (p.Gly81Cys) | ClinVar dbSNP |
| 17 | g.48728353C= | CA2263242621 | HOXB13 | c.241G= (p.Gly81=) | |
| 17 | g.48728353C>G | CA400107859 | HOXB13 | c.241G>C (p.Gly81Arg) | |
| 17 | g.48728353C>T | CA400107860 | HOXB13 | c.241G>A (p.Gly81Ser) | |
| 17 | g.48728354A= | CA2263242622 | HOXB13 | c.240T= (p.Tyr80=) | |
| 17 | g.48728354A>C | CA400107862 | HOXB13 | c.240T>G (p.Tyr80Ter) | |
| 17 | g.48728354A>G | CA500661996 | HOXB13 | c.240T>C (p.Tyr80=) | ClinVar dbSNP |
| 17 | g.48728354A>T | CA400107861 | HOXB13 | c.240T>A (p.Tyr80Ter) | ClinVar dbSNP gnomAD v3 gnomAD v4 |