| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.4862718G>A | CA356138215 | MSX1 | c.487G>A (p.Ala163Thr) n.199G>A | |
| 4 | g.4862718G>C | CA356138214 | MSX1 | c.487G>C (p.Ala163Pro) n.199G>C | gnomAD v4 |
| 4 | g.4862718G= | CA1435013619 | MSX1 | c.487G= (p.Ala163=) n.199G= | |
| 4 | g.4862718G>T | CA2833060 | MSX1 | c.487G>T (p.Ala163Ser) n.199G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862718dup | CA2580070729 | MSX1 | c.487dup (p.Ala163GlyfsTer12) n.199dup | ClinVar |
| 4 | g.4862719C>A | CA356138218 | MSX1 | c.488C>A (p.Ala163Asp) n.200C>A | |
| 4 | g.4862719C= | CA1435013620 | MSX1 | c.488C= (p.Ala163=) n.200C= | |
| 4 | g.4862719C>G | CA356138216 | MSX1 | c.488C>G (p.Ala163Gly) n.200C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.4862719C>T | CA356138217 | MSX1 | c.488C>T (p.Ala163Val) n.200C>T | dbSNP |
| 4 | g.4862720C>A | CA438365928 | MSX1 | c.489C>A (p.Ala163=) n.201C>A | |
| 4 | g.4862720C>G | CA438365929 | MSX1 | c.489C>G (p.Ala163=) n.201C>G | |
| 4 | g.4862720C>T | CA438365930 | MSX1 | c.489C>T (p.Ala163=) n.201C>T | gnomAD v4 |
| 4 | g.4862721T>A | CA356138219 | MSX1 | c.490T>A (p.Cys164Ser) n.202T>A | dbSNP |
| 4 | g.4862721T>C | CA356138220 | MSX1 | c.490T>C (p.Cys164Arg) n.202T>C | |
| 4 | g.4862721T>G | CA356138221 | MSX1 | c.490T>G (p.Cys164Gly) n.202T>G | gnomAD v4 |
| 4 | g.4862721T= | CA1435013621 | MSX1 | c.490T= (p.Cys164=) n.202T= | |
| 4 | g.4862722G>A | CA356138222 | MSX1 | c.491G>A (p.Cys164Tyr) n.203G>A | |
| 4 | g.4862722G>C | CA356138223 | MSX1 | c.491G>C (p.Cys164Ser) n.203G>C | |
| 4 | g.4862722G>T | CA356138224 | MSX1 | c.491G>T (p.Cys164Phe) n.203G>T | gnomAD v4 |
| 4 | g.4862723C>A | CA356138225 | MSX1 | c.492C>A (p.Cys164Ter) n.204C>A | |
| 4 | g.4862723C>G | CA356138226 | MSX1 | c.492C>G (p.Cys164Trp) n.204C>G | |
| 4 | g.4862723C>T | CA438365931 | MSX1 | c.492C>T (p.Cys164=) n.204C>T | |
| 4 | g.4862724A= | CA1435013622 | MSX1 | c.493A= (p.Thr165=) n.205A= | |
| 4 | g.4862724A>C | CA356138227 | MSX1 | c.493A>C (p.Thr165Pro) n.205A>C | dbSNP |
| 4 | g.4862724A>G | CA356138228 | MSX1 | c.493A>G (p.Thr165Ala) n.205A>G | |
| 4 | g.4862724A>T | CA356138229 | MSX1 | c.493A>T (p.Thr165Ser) n.205A>T | |
| 4 | g.4862725C>A | CA356138232 | MSX1 | c.494C>A (p.Thr165Asn) n.206C>A | |
| 4 | g.4862725C>G | CA356138231 | MSX1 | c.494C>G (p.Thr165Ser) n.206C>G | |
| 4 | g.4862725C>T | CA356138230 | MSX1 | c.494C>T (p.Thr165Ile) n.206C>T | |
| 4 | g.4862726C>A | CA438365932 | MSX1 | c.495C>A (p.Thr165=) n.207C>A | |
| 4 | g.4862726C>G | CA438365934 | MSX1 | c.495C>G (p.Thr165=) n.207C>G | gnomAD v4 |
| 4 | g.4862726C>T | CA438365935 | MSX1 | c.495C>T (p.Thr165=) n.207C>T | |
| 4 | g.4862727C>A | CA356138233 | MSX1 | c.496C>A (p.Leu166Ile) n.208C>A | |
| 4 | g.4862727C>G | CA356138234 | MSX1 | c.496C>G (p.Leu166Val) n.208C>G | |
| 4 | g.4862727C>T | CA356138235 | MSX1 | c.496C>T (p.Leu166Phe) n.208C>T | gnomAD v4 |
| 4 | g.4862728T>A | CA356138236 | MSX1 | c.497T>A (p.Leu166His) n.209T>A | |
| 4 | g.4862728T>C | CA356138237 | MSX1 | c.497T>C (p.Leu166Pro) n.209T>C | dbSNP |
| 4 | g.4862728T>G | CA356138238 | MSX1 | c.497T>G (p.Leu166Arg) n.209T>G | |
| 4 | g.4862728T= | CA1435013623 | MSX1 | c.497T= (p.Leu166=) n.209T= | |
| 4 | g.4862729C>A | CA438365938 | MSX1 | c.498C>A (p.Leu166=) n.210C>A | |
| 4 | g.4862729C= | CA1435013624 | MSX1 | c.498C= (p.Leu166=) n.210C= | |
| 4 | g.4862729C>G | CA438365939 | MSX1 | c.498C>G (p.Leu166=) n.210C>G | |
| 4 | g.4862729C>T | CA438365941 | MSX1 | c.498C>T (p.Leu166=) n.210C>T | dbSNP |
| 4 | g.4862730C>A | CA356138239 | MSX1 | c.499C>A (p.Arg167Ser) n.211C>A | |
| 4 | g.4862730C= | CA1435013625 | MSX1 | c.499C= (p.Arg167=) n.211C= | |
| 4 | g.4862730C>G | CA356138240 | MSX1 | c.499C>G (p.Arg167Gly) n.211C>G | |
| 4 | g.4862730C>T | CA91671821 | MSX1 | c.499C>T (p.Arg167Cys) n.211C>T | dbSNP gnomAD v4 COSMIC |
| 4 | g.4862731G>A | CA356138241 | MSX1 | c.500G>A (p.Arg167His) n.212G>A | gnomAD v4 |
| 4 | g.4862731G>C | CA356138242 | MSX1 | c.500G>C (p.Arg167Pro) n.212G>C | COSMIC |
| 4 | g.4862731G>T | CA356138243 | MSX1 | c.500G>T (p.Arg167Leu) n.212G>T |