| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.74740902C>A | CA413665049 | NEXMIF | c.3655G>T (p.Val1219Phe) | |
| X | g.74740902C>G | CA413665051 | NEXMIF | c.3655G>C (p.Val1219Leu) | |
| X | g.74740902C>T | CA413665047 | NEXMIF | c.3655G>A (p.Val1219Ile) | ClinVar |
| X | g.74740903C>A | CA413665055 | NEXMIF | c.3654G>T (p.Gln1218His) | |
| X | g.74740903C>G | CA413665056 | NEXMIF | c.3654G>C (p.Gln1218His) | gnomAD v4 |
| X | g.74740903C>T | CA517466546 | NEXMIF | c.3654G>A (p.Gln1218=) | gnomAD v4 |
| X | g.74740904T>A | CA413665057 | NEXMIF | c.3653A>T (p.Gln1218Leu) | |
| X | g.74740904T>C | CA331301712 | NEXMIF | c.3653A>G (p.Gln1218Arg) | ClinVar dbSNP |
| X | g.74740904T>G | CA413665059 | NEXMIF | c.3653A>C (p.Gln1218Pro) | |
| X | g.74740904T= | CA2437590163 | NEXMIF | c.3653A= (p.Gln1218=) | |
| X | g.74740905G>A | CA413665065 | NEXMIF | c.3652C>T (p.Gln1218Ter) | COSMIC |
| X | g.74740905G>C | CA413665063 | NEXMIF | c.3652C>G (p.Gln1218Glu) | |
| X | g.74740905G>T | CA413665062 | NEXMIF | c.3652C>A (p.Gln1218Lys) | |
| X | g.74740906G>A | CA517466550 | NEXMIF | c.3651C>T (p.Arg1217=) | |
| X | g.74740906G>C | CA517466551 | NEXMIF | c.3651C>G (p.Arg1217=) | |
| X | g.74740906G>T | CA517466552 | NEXMIF | c.3651C>A (p.Arg1217=) | |
| X | g.74740907C>A | CA413665067 | NEXMIF | c.3650G>T (p.Arg1217Leu) | dbSNP |
| X | g.74740907C= | CA2437590164 | NEXMIF | c.3650G= (p.Arg1217=) | |
| X | g.74740907C>G | CA413665069 | NEXMIF | c.3650G>C (p.Arg1217Pro) | |
| X | g.74740907C>T | CA10454921 | NEXMIF | c.3650G>A (p.Arg1217His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| X | g.74740908G>A | CA331301713 | NEXMIF | c.3649C>T (p.Arg1217Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| X | g.74740908G>C | CA413665072 | NEXMIF | c.3649C>G (p.Arg1217Gly) | |
| X | g.74740908G= | CA2437590165 | NEXMIF | c.3649C= (p.Arg1217=) | |
| X | g.74740908G>T | CA413665074 | NEXMIF | c.3649C>A (p.Arg1217Ser) | |
| X | g.74740909G>A | CA10454922 | NEXMIF | c.3648C>T (p.Ser1216=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.74740909G>C | CA517466557 | NEXMIF | c.3648C>G (p.Ser1216=) | |
| X | g.74740909G= | CA2437590166 | NEXMIF | c.3648C= (p.Ser1216=) | |
| X | g.74740909G>T | CA517466558 | NEXMIF | c.3648C>A (p.Ser1216=) | |
| X | g.74740910G>A | CA413665080 | NEXMIF | c.3647C>T (p.Ser1216Phe) | |
| X | g.74740910G>C | CA413665079 | NEXMIF | c.3647C>G (p.Ser1216Cys) | |
| X | g.74740910G>T | CA413665077 | NEXMIF | c.3647C>A (p.Ser1216Tyr) | |
| X | g.74740911A>C | CA413665084 | NEXMIF | c.3646T>G (p.Ser1216Ala) | |
| X | g.74740911A>G | CA413665082 | NEXMIF | c.3646T>C (p.Ser1216Pro) | |
| X | g.74740911A>T | CA413665086 | NEXMIF | c.3646T>A (p.Ser1216Thr) | |
| X | g.74740912G>A | CA517466562 | NEXMIF | c.3645C>T (p.Asn1215=) | |
| X | g.74740912G>C | CA413665088 | NEXMIF | c.3645C>G (p.Asn1215Lys) | |
| X | g.74740912G>T | CA413665090 | NEXMIF | c.3645C>A (p.Asn1215Lys) | |
| X | g.74740913T>A | CA413665092 | NEXMIF | c.3644A>T (p.Asn1215Ile) | |
| X | g.74740913T>C | CA413665094 | NEXMIF | c.3644A>G (p.Asn1215Ser) | |
| X | g.74740913T>G | CA331301714 | NEXMIF | c.3644A>C (p.Asn1215Thr) | dbSNP |
| X | g.74740913T= | CA2437590167 | NEXMIF | c.3644A= (p.Asn1215=) | |
| X | g.74740914T>A | CA413665096 | NEXMIF | c.3643A>T (p.Asn1215Tyr) | |
| X | g.74740914T>C | CA413665099 | NEXMIF | c.3643A>G (p.Asn1215Asp) | |
| X | g.74740914T>G | CA413665098 | NEXMIF | c.3643A>C (p.Asn1215His) | |
| X | g.74740915T>A | CA413665101 | NEXMIF | c.3642A>T (p.Lys1214Asn) | |
| X | g.74740915T>C | CA517466565 | NEXMIF | c.3642A>G (p.Lys1214=) | |
| X | g.74740915T>G | CA413665104 | NEXMIF | c.3642A>C (p.Lys1214Asn) | |
| X | g.74740916T>A | CA413665106 | NEXMIF | c.3641A>T (p.Lys1214Ile) | |
| X | g.74740916T>C | CA413665107 | NEXMIF | c.3641A>G (p.Lys1214Arg) | ClinVar |
| X | g.74740916T>G | CA413665109 | NEXMIF | c.3641A>C (p.Lys1214Thr) |