Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.74740853T>A | CA413664933 | NEXMIF | c.3704A>T (p.Glu1235Val) | |
X | g.74740853T>C | CA413664934 | NEXMIF | c.3704A>G (p.Glu1235Gly) | |
X | g.74740853T>G | CA413664935 | NEXMIF | c.3704A>C (p.Glu1235Ala) | |
X | g.74740854C>A | CA413664936 | NEXMIF | c.3703G>T (p.Glu1235Ter) | |
X | g.74740854C= | CA2437590140 | NEXMIF | c.3703G= (p.Glu1235=) | |
X | g.74740854C>G | CA413664937 | NEXMIF | c.3703G>C (p.Glu1235Gln) | |
X | g.74740854C>T | CA10454918 | NEXMIF | c.3703G>A (p.Glu1235Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.74740855T>A | CA517466448 | NEXMIF | c.3702A>T (p.Gly1234=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.74740855T>C | CA517466450 | NEXMIF | c.3702A>G (p.Gly1234=) | |
X | g.74740855T>G | CA517466453 | NEXMIF | c.3702A>C (p.Gly1234=) | |
X | g.74740855T= | CA2437590141 | NEXMIF | c.3702A= (p.Gly1234=) | |
X | g.74740856C>A | CA413664938 | NEXMIF | c.3701G>T (p.Gly1234Val) | |
X | g.74740856C= | CA2437590142 | NEXMIF | c.3701G= (p.Gly1234=) | |
X | g.74740856C>G | CA413664939 | NEXMIF | c.3701G>C (p.Gly1234Ala) | |
X | g.74740856C>T | CA10454919 | NEXMIF | c.3701G>A (p.Gly1234Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.74740857C>A | CA413664940 | NEXMIF | c.3700G>T (p.Gly1234Ter) | ClinVar dbSNP |
X | g.74740857C= | CA2437590143 | NEXMIF | c.3700G= (p.Gly1234=) | |
X | g.74740857C>G | CA413664942 | NEXMIF | c.3700G>C (p.Gly1234Arg) | |
X | g.74740857C>T | CA413664941 | NEXMIF | c.3700G>A (p.Gly1234Arg) | dbSNP gnomAD v2 gnomAD v4 |
X | g.74740858A= | CA2437590144 | NEXMIF | c.3699T= (p.Asn1233=) | |
X | g.74740858A>C | CA413664943 | NEXMIF | c.3699T>G (p.Asn1233Lys) | |
X | g.74740858A>G | CA517466455 | NEXMIF | c.3699T>C (p.Asn1233=) | dbSNP gnomAD v4 |
X | g.74740858A>T | CA413664944 | NEXMIF | c.3699T>A (p.Asn1233Lys) | |
X | g.74740859T>A | CA413664945 | NEXMIF | c.3698A>T (p.Asn1233Ile) | |
X | g.74740859T>C | CA413664946 | NEXMIF | c.3698A>G (p.Asn1233Ser) | |
X | g.74740859T>G | CA413664947 | NEXMIF | c.3698A>C (p.Asn1233Thr) | |
X | g.74740860T>A | CA413664948 | NEXMIF | c.3697A>T (p.Asn1233Tyr) | |
X | g.74740860T>C | CA413664949 | NEXMIF | c.3697A>G (p.Asn1233Asp) | |
X | g.74740860T>G | CA413664950 | NEXMIF | c.3697A>C (p.Asn1233His) | |
X | g.74740861G>A | CA517466457 | NEXMIF | c.3696C>T (p.Ile1232=) | dbSNP |
X | g.74740861G>C | CA413664951 | NEXMIF | c.3696C>G (p.Ile1232Met) | |
X | g.74740861G= | CA2437590145 | NEXMIF | c.3696C= (p.Ile1232=) | |
X | g.74740861G>T | CA517466459 | NEXMIF | c.3696C>A (p.Ile1232=) | |
X | g.74740862A>C | CA413664952 | NEXMIF | c.3695T>G (p.Ile1232Ser) | |
X | g.74740862A>G | CA413664953 | NEXMIF | c.3695T>C (p.Ile1232Thr) | |
X | g.74740862A>T | CA413664954 | NEXMIF | c.3695T>A (p.Ile1232Asn) | |
X | g.74740863T>A | CA413664956 | NEXMIF | c.3694A>T (p.Ile1232Phe) | |
X | g.74740863T>C | CA331301709 | NEXMIF | c.3694A>G (p.Ile1232Val) | dbSNP gnomAD v3 gnomAD v4 |
X | g.74740863T>G | CA413664955 | NEXMIF | c.3694A>C (p.Ile1232Leu) | |
X | g.74740863T= | CA2437590146 | NEXMIF | c.3694A= (p.Ile1232=) | |
X | g.74740864G>A | CA517466466 | NEXMIF | c.3693C>T (p.Ala1231=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.74740864G>C | CA517466465 | NEXMIF | c.3693C>G (p.Ala1231=) | |
X | g.74740864G= | CA2437590147 | NEXMIF | c.3693C= (p.Ala1231=) | |
X | g.74740864G>T | CA517466463 | NEXMIF | c.3693C>A (p.Ala1231=) | |
X | g.74740865G>A | CA413664957 | NEXMIF | c.3692C>T (p.Ala1231Val) | |
X | g.74740865G>C | CA413664958 | NEXMIF | c.3692C>G (p.Ala1231Gly) | |
X | g.74740865G>T | CA413664959 | NEXMIF | c.3692C>A (p.Ala1231Asp) | |
X | g.74740866C>A | CA413664960 | NEXMIF | c.3691G>T (p.Ala1231Ser) | ClinVar dbSNP gnomAD v4 |
X | g.74740866C= | CA2437590148 | NEXMIF | c.3691G= (p.Ala1231=) | |
X | g.74740866C>G | CA413664961 | NEXMIF | c.3691G>C (p.Ala1231Pro) |