Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.74741002C>A | CA10454932 | NEXMIF | c.3555G>T (p.Gly1185=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.74741002C= | CA2437590199 | NEXMIF | c.3555G= (p.Gly1185=) | |
X | g.74741002C>G | CA517466147 | NEXMIF | c.3555G>C (p.Gly1185=) | |
X | g.74741002C>T | CA517466148 | NEXMIF | c.3555G>A (p.Gly1185=) | |
X | g.74741003C>A | CA413665454 | NEXMIF | c.3554G>T (p.Gly1185Val) | |
X | g.74741003C>G | CA413665450 | NEXMIF | c.3554G>C (p.Gly1185Ala) | |
X | g.74741003C>T | CA413665452 | NEXMIF | c.3554G>A (p.Gly1185Glu) | |
X | g.74741004C>A | CA413665456 | NEXMIF | c.3553G>T (p.Gly1185Trp) | COSMIC |
X | g.74741004C>G | CA413665457 | NEXMIF | c.3553G>C (p.Gly1185Arg) | |
X | g.74741004C>T | CA413665458 | NEXMIF | c.3553G>A (p.Gly1185Arg) | |
X | g.74741005A>C | CA413665459 | NEXMIF | c.3552T>G (p.Ser1184Arg) | |
X | g.74741005A>G | CA517466150 | NEXMIF | c.3552T>C (p.Ser1184=) | |
X | g.74741005A>T | CA413665460 | NEXMIF | c.3552T>A (p.Ser1184Arg) | |
X | g.74741006C>A | CA413665464 | NEXMIF | c.3551G>T (p.Ser1184Ile) | |
X | g.74741006C= | CA2437590200 | NEXMIF | c.3551G= (p.Ser1184=) | |
X | g.74741006C>G | CA413665466 | NEXMIF | c.3551G>C (p.Ser1184Thr) | |
X | g.74741006C>T | CA413665468 | NEXMIF | c.3551G>A (p.Ser1184Asn) | dbSNP gnomAD v2 gnomAD v4 |
X | g.74741007T>A | CA413665470 | NEXMIF | c.3550A>T (p.Ser1184Cys) | |
X | g.74741007T>C | CA413665471 | NEXMIF | c.3550A>G (p.Ser1184Gly) | |
X | g.74741007T>G | CA413665473 | NEXMIF | c.3550A>C (p.Ser1184Arg) | |
X | g.74741008C>A | CA413665476 | NEXMIF | c.3549G>T (p.Lys1183Asn) | |
X | g.74741008C>G | CA413665475 | NEXMIF | c.3549G>C (p.Lys1183Asn) | |
X | g.74741008C>T | CA517466154 | NEXMIF | c.3549G>A (p.Lys1183=) | |
X | g.74741009T>A | CA413665478 | NEXMIF | c.3548A>T (p.Lys1183Met) | |
X | g.74741009T>C | CA413665480 | NEXMIF | c.3548A>G (p.Lys1183Arg) | |
X | g.74741009T>G | CA413665482 | NEXMIF | c.3548A>C (p.Lys1183Thr) | |
X | g.74741010T>A | CA413665484 | NEXMIF | c.3547A>T (p.Lys1183Ter) | |
X | g.74741010T>C | CA413665487 | NEXMIF | c.3547A>G (p.Lys1183Glu) | |
X | g.74741010T>G | CA413665489 | NEXMIF | c.3547A>C (p.Lys1183Gln) | |
X | g.74741011G>A | CA517466155 | NEXMIF | c.3546C>T (p.Ser1182=) | |
X | g.74741011G>C | CA413665491 | NEXMIF | c.3546C>G (p.Ser1182Arg) | dbSNP gnomAD v4 |
X | g.74741011G= | CA2437590201 | NEXMIF | c.3546C= (p.Ser1182=) | |
X | g.74741011G>T | CA413665492 | NEXMIF | c.3546C>A (p.Ser1182Arg) | |
X | g.74741012C>A | CA10454933 | NEXMIF | c.3545G>T (p.Ser1182Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.74741012C= | CA2437590202 | NEXMIF | c.3545G= (p.Ser1182=) | |
X | g.74741012C>G | CA413665494 | NEXMIF | c.3545G>C (p.Ser1182Thr) | |
X | g.74741012C>T | CA413665495 | NEXMIF | c.3545G>A (p.Ser1182Asn) | gnomAD v4 |
X | g.74741013T>A | CA413665496 | NEXMIF | c.3544A>T (p.Ser1182Cys) | |
X | g.74741013T>C | CA413665498 | NEXMIF | c.3544A>G (p.Ser1182Gly) | |
X | g.74741013T>G | CA413665499 | NEXMIF | c.3544A>C (p.Ser1182Arg) | |
X | g.74741014G>A | CA517466159 | NEXMIF | c.3543C>T (p.Pro1181=) | |
X | g.74741014G>C | CA517466160 | NEXMIF | c.3543C>G (p.Pro1181=) | COSMIC |
X | g.74741014G>T | CA517466158 | NEXMIF | c.3543C>A (p.Pro1181=) | gnomAD v4 |
X | g.74741015G>A | CA413665502 | NEXMIF | c.3542C>T (p.Pro1181Leu) | gnomAD v4 |
X | g.74741015G>C | CA413665504 | NEXMIF | c.3542C>G (p.Pro1181Arg) | dbSNP |
X | g.74741015G= | CA2437590203 | NEXMIF | c.3542C= (p.Pro1181=) | |
X | g.74741015G>T | CA413665501 | NEXMIF | c.3542C>A (p.Pro1181His) | |
X | g.74741016G>A | CA413665506 | NEXMIF | c.3541C>T (p.Pro1181Ser) | |
X | g.74741016G>C | CA413665509 | NEXMIF | c.3541C>G (p.Pro1181Ala) | gnomAD v4 |
X | g.74741016G>T | CA413665508 | NEXMIF | c.3541C>A (p.Pro1181Thr) |