| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.74740848T>A | CA10454917 | NEXMIF | c.3709A>T (p.Met1237Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.74740848T>C | CA413664921 | NEXMIF | c.3709A>G (p.Met1237Val) | |
| X | g.74740848T>G | CA413664922 | NEXMIF | c.3709A>C (p.Met1237Leu) | |
| X | g.74740848T= | CA2437590139 | NEXMIF | c.3709A= (p.Met1237=) | |
| X | g.74740851dup | CA2573055403 | NEXMIF | c.3709dup (p.Met1237AsnfsTer24) | ClinVar dbSNP |
| X | g.74740849T>A | CA413664923 | NEXMIF | c.3708A>T (p.Lys1236Asn) | |
| X | g.74740849T>C | CA517466430 | NEXMIF | c.3708A>G (p.Lys1236=) | |
| X | g.74740849T>G | CA413664924 | NEXMIF | c.3708A>C (p.Lys1236Asn) | |
| X | g.74740850T>A | CA413664925 | NEXMIF | c.3707A>T (p.Lys1236Ile) | |
| X | g.74740850T>C | CA413664927 | NEXMIF | c.3707A>G (p.Lys1236Arg) | |
| X | g.74740850T>G | CA413664926 | NEXMIF | c.3707A>C (p.Lys1236Thr) | |
| X | g.74740851T>A | CA413664928 | NEXMIF | c.3706A>T (p.Lys1236Ter) | |
| X | g.74740851T>C | CA413664929 | NEXMIF | c.3706A>G (p.Lys1236Glu) | COSMIC |
| X | g.74740851T>G | CA413664930 | NEXMIF | c.3706A>C (p.Lys1236Gln) | |
| X | g.74740852C>A | CA413664931 | NEXMIF | c.3705G>T (p.Glu1235Asp) | |
| X | g.74740852C>G | CA413664932 | NEXMIF | c.3705G>C (p.Glu1235Asp) | |
| X | g.74740852C>T | CA517466441 | NEXMIF | c.3705G>A (p.Glu1235=) | |
| 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=) |