Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.4860241G>A | CA438365840 | MSX1 | c.342G>A (p.Pro114=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.4860241G>C | CA438365842 | MSX1 | c.342G>C (p.Pro114=) | |
4 | g.4860241G= | CA1435012209 | MSX1 | c.342G= (p.Pro114=) | |
4 | g.4860241G>T | CA438365844 | MSX1 | c.342G>T (p.Pro114=) | gnomAD v4 |
4 | g.4860242C>A | CA356137802 | MSX1 | c.343C>A (p.Leu115Ile) | |
4 | g.4860242C>G | CA356137804 | MSX1 | c.343C>G (p.Leu115Val) | |
4 | g.4860242C>T | CA356137806 | MSX1 | c.343C>T (p.Leu115Phe) | |
4 | g.4860243T>A | CA356137808 | MSX1 | c.344T>A (p.Leu115His) | |
4 | g.4860243T>C | CA356137810 | MSX1 | c.344T>C (p.Leu115Pro) | gnomAD v4 |
4 | g.4860243T>G | CA356137812 | MSX1 | c.344T>G (p.Leu115Arg) | |
4 | g.4860244C>A | CA438365846 | MSX1 | c.345C>A (p.Leu115=) | gnomAD v4 |
4 | g.4860244C= | CA1435012210 | MSX1 | c.345C= (p.Leu115=) | |
4 | g.4860244C>G | CA438365848 | MSX1 | c.345C>G (p.Leu115=) | |
4 | g.4860244C>T | CA438365847 | MSX1 | c.345C>T (p.Leu115=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
4 | g.4860245G>A | CA356137814 | MSX1 | c.346G>A (p.Gly116Ser) | gnomAD v4 |
4 | g.4860245G>C | CA356137818 | MSX1 | c.346G>C (p.Gly116Arg) | gnomAD v4 |
4 | g.4860245G>T | CA356137816 | MSX1 | c.346G>T (p.Gly116Cys) | gnomAD v4 |
4 | g.4860246G>A | CA356137819 | MSX1 | c.347G>A (p.Gly116Asp) | gnomAD v4 |
4 | g.4860246G>C | CA356137820 | MSX1 | c.347G>C (p.Gly116Ala) | |
4 | g.4860246G= | CA1435012211 | MSX1 | c.347G= (p.Gly116=) | |
4 | g.4860246G>T | CA356137822 | MSX1 | c.347G>T (p.Gly116Val) | dbSNP gnomAD v4 |
4 | g.4860247C>A | CA438365850 | MSX1 | c.348C>A (p.Gly116=) | |
4 | g.4860247C= | CA1435012212 | MSX1 | c.348C= (p.Gly116=) | |
4 | g.4860247C>G | CA438365851 | MSX1 | c.348C>G (p.Gly116=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.4860247C>T | CA2832948 | MSX1 | c.348C>T (p.Gly116=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4860248C>A | CA356137824 | MSX1 | c.349C>A (p.His117Asn) | gnomAD v4 |
4 | g.4860248C= | CA1435012213 | MSX1 | c.349C= (p.His117=) | |
4 | g.4860248C>G | CA356137825 | MSX1 | c.349C>G (p.His117Asp) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.4860248C>T | CA356137826 | MSX1 | c.349C>T (p.His117Tyr) | dbSNP gnomAD v4 |
4 | g.4860249A= | CA1435012214 | MSX1 | c.350A= (p.His117=) | |
4 | g.4860249A>C | CA356137828 | MSX1 | c.350A>C (p.His117Pro) | |
4 | g.4860249A>G | CA356137830 | MSX1 | c.350A>G (p.His117Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4860249A>T | CA91668764 | MSX1 | c.350A>T (p.His117Leu) | dbSNP |
4 | g.4860250T>A | CA356137832 | MSX1 | c.351T>A (p.His117Gln) | |
4 | g.4860250T>C | CA438365855 | MSX1 | c.351T>C (p.His117=) | |
4 | g.4860250T>G | CA356137834 | MSX1 | c.351T>G (p.His117Gln) | |
4 | g.4860251T>A | CA356137839 | MSX1 | c.352T>A (p.Phe118Ile) | |
4 | g.4860251T>C | CA356137836 | MSX1 | c.352T>C (p.Phe118Leu) | |
4 | g.4860251T>G | CA356137838 | MSX1 | c.352T>G (p.Phe118Val) | |
4 | g.4860252T>A | CA356137842 | MSX1 | c.353T>A (p.Phe118Tyr) | |
4 | g.4860252T>C | CA356137843 | MSX1 | c.353T>C (p.Phe118Ser) | |
4 | g.4860252T>G | CA356137845 | MSX1 | c.353T>G (p.Phe118Cys) | |
4 | g.4860253C>A | CA356137846 | MSX1 | c.354C>A (p.Phe118Leu) | gnomAD v4 |
4 | g.4860253C= | CA1435012215 | MSX1 | c.354C= (p.Phe118=) | |
4 | g.4860253C>G | CA356137847 | MSX1 | c.354C>G (p.Phe118Leu) | |
4 | g.4860253C>T | CA438365857 | MSX1 | c.354C>T (p.Phe118=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4860254T>A | CA356137849 | MSX1 | c.355T>A (p.Ser119Thr) | |
4 | g.4860254T>C | CA356137850 | MSX1 | c.355T>C (p.Ser119Pro) | |
4 | g.4860254T>G | CA356137852 | MSX1 | c.355T>G (p.Ser119Ala) | |
4 | g.4860255C>A | CA356137854 | MSX1 | c.356C>A (p.Ser119Ter) | gnomAD v4 |