| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.4862750_4862756dup | CA2573052331 | MSX1 | c.519_525dup (p.Arg176Ter) n.231_237dup | ClinVar dbSNP |
| 4 | g.4862754C>A | CA356138290 | MSX1 | c.523C>A (p.Pro175Thr) n.235C>A | gnomAD v4 |
| 4 | g.4862754C>G | CA356138291 | MSX1 | c.523C>G (p.Pro175Ala) n.235C>G | |
| 4 | g.4862754C>T | CA356138292 | MSX1 | c.523C>T (p.Pro175Ser) n.235C>T | |
| 4 | g.4862755C>A | CA356138293 | MSX1 | c.524C>A (p.Pro175Gln) n.236C>A | |
| 4 | g.4862755C= | CA1435013638 | MSX1 | c.524C= (p.Pro175=) n.236C= | |
| 4 | g.4862755C>G | CA356138294 | MSX1 | c.524C>G (p.Pro175Arg) n.236C>G | |
| 4 | g.4862755C>T | CA91671931 | MSX1 | c.524C>T (p.Pro175Leu) n.236C>T | dbSNP |
| 4 | g.4862756G>A | CA91671934 | MSX1 | c.525G>A (p.Pro175=) n.237G>A | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.4862756G>C | CA438365967 | MSX1 | c.525G>C (p.Pro175=) n.237G>C | |
| 4 | g.4862756G= | CA1435013639 | MSX1 | c.525G= (p.Pro175=) n.237G= | |
| 4 | g.4862756G>T | CA438365966 | MSX1 | c.525G>T (p.Pro175=) n.237G>T | |
| 4 | g.4862757C>A | CA438365968 | MSX1 | c.526C>A (p.Arg176=) n.238C>A | ClinVar dbSNP |
| 4 | g.4862757C= | CA1435013640 | MSX1 | c.526C= (p.Arg176=) n.238C= | |
| 4 | g.4862757C>G | CA356138295 | MSX1 | c.526C>G (p.Arg176Gly) n.238C>G | |
| 4 | g.4862757C>T | CA356138296 | MSX1 | c.526C>T (p.Arg176Trp) n.238C>T | gnomAD v4 COSMIC |
| 4 | g.4862758G>A | CA356138299 | MSX1 | c.527G>A (p.Arg176Gln) n.239G>A | ClinVar COSMIC |
| 4 | g.4862758G>C | CA356138298 | MSX1 | c.527G>C (p.Arg176Pro) n.239G>C | |
| 4 | g.4862758G>T | CA356138297 | MSX1 | c.527G>T (p.Arg176Leu) n.239G>T | |
| 4 | g.4862759G>A | CA438365971 | MSX1 | c.528G>A (p.Arg176=) n.240G>A | |
| 4 | g.4862759G>C | CA438365972 | MSX1 | c.528G>C (p.Arg176=) n.240G>C | |
| 4 | g.4862759G>T | CA438365973 | MSX1 | c.528G>T (p.Arg176=) n.240G>T | |
| 4 | g.4862760A>C | CA356138302 | MSX1 | c.529A>C (p.Thr177Pro) n.241A>C | |
| 4 | g.4862760A>G | CA356138300 | MSX1 | c.529A>G (p.Thr177Ala) n.241A>G | |
| 4 | g.4862760A>T | CA356138301 | MSX1 | c.529A>T (p.Thr177Ser) n.241A>T | |
| 4 | g.4862761C>A | CA356138303 | MSX1 | c.530C>A (p.Thr177Lys) n.242C>A | |
| 4 | g.4862761C>G | CA356138304 | MSX1 | c.530C>G (p.Thr177Arg) n.242C>G | |
| 4 | g.4862761C>T | CA356138305 | MSX1 | c.530C>T (p.Thr177Met) n.242C>T | |
| 4 | g.4862762G>A | CA2833068 | MSX1 | c.531G>A (p.Thr177=) n.243G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 4 | g.4862762G>C | CA438365976 | MSX1 | c.531G>C (p.Thr177=) n.243G>C | |
| 4 | g.4862762G= | CA1435013641 | MSX1 | c.531G= (p.Thr177=) n.243G= | |
| 4 | g.4862762G>T | CA438365977 | MSX1 | c.531G>T (p.Thr177=) n.243G>T | dbSNP |
| 4 | g.4862763C>A | CA356138306 | MSX1 | c.532C>A (p.Pro178Thr) n.244C>A | |
| 4 | g.4862763C>G | CA356138307 | MSX1 | c.532C>G (p.Pro178Ala) n.244C>G | gnomAD v4 |
| 4 | g.4862763C>T | CA356138308 | MSX1 | c.532C>T (p.Pro178Ser) n.244C>T | gnomAD v4 |
| 4 | g.4862764C>A | CA356138309 | MSX1 | c.533C>A (p.Pro178His) n.245C>A | |
| 4 | g.4862764C>G | CA356138310 | MSX1 | c.533C>G (p.Pro178Arg) n.245C>G | |
| 4 | g.4862764C>T | CA356138311 | MSX1 | c.533C>T (p.Pro178Leu) n.245C>T | gnomAD v4 |
| 4 | g.4862765C>A | CA438365980 | MSX1 | c.534C>A (p.Pro178=) n.246C>A | |
| 4 | g.4862765C>G | CA438365979 | MSX1 | c.534C>G (p.Pro178=) n.246C>G | |
| 4 | g.4862765C>T | CA438365978 | MSX1 | c.534C>T (p.Pro178=) n.246C>T | dbSNP |
| 4 | g.4862766T>A | CA356138313 | MSX1 | c.535T>A (p.Phe179Ile) n.247T>A | dbSNP |
| 4 | g.4862766T>C | CA356138314 | MSX1 | c.535T>C (p.Phe179Leu) n.247T>C | |
| 4 | g.4862766T>G | CA356138312 | MSX1 | c.535T>G (p.Phe179Val) n.247T>G | |
| 4 | g.4862766T= | CA1435013642 | MSX1 | c.535T= (p.Phe179=) n.247T= | |
| 4 | g.4862767T>A | CA356138315 | MSX1 | c.536T>A (p.Phe179Tyr) n.248T>A | |
| 4 | g.4862767T>C | CA356138316 | MSX1 | c.536T>C (p.Phe179Ser) n.248T>C | |
| 4 | g.4862767T>G | CA356138317 | MSX1 | c.536T>G (p.Phe179Cys) n.248T>G | COSMIC |
| 4 | g.4862768C>A | CA356138318 | MSX1 | c.537C>A (p.Phe179Leu) n.249C>A | dbSNP |
| 4 | g.4862768C= | CA1435013643 | MSX1 | c.537C= (p.Phe179=) n.249C= |