ClinVar Miner

List of variants reported as uncertain significance for Vitamin K-dependent clotting factors, combined deficiency of, 1

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ClinVar version:
Total variants: 135
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HGVS dbSNP
NM_000821.7(GGCX):c.*1019G>C rs545427723
NM_000821.7(GGCX):c.*1037A>G
NM_000821.7(GGCX):c.*106T>G rs530539627
NM_000821.7(GGCX):c.*107T>G rs78909830
NM_000821.7(GGCX):c.*108G>T rs886056378
NM_000821.7(GGCX):c.*1145G>A
NM_000821.7(GGCX):c.*1186A>G rs886056372
NM_000821.7(GGCX):c.*1245G>C rs190566964
NM_000821.7(GGCX):c.*1324T>C
NM_000821.7(GGCX):c.*1367C>A
NM_000821.7(GGCX):c.*1604G>A
NM_000821.7(GGCX):c.*1686C>G
NM_000821.7(GGCX):c.*1698A>G rs143548117
NM_000821.7(GGCX):c.*1712A>C
NM_000821.7(GGCX):c.*1721G>A rs187452629
NM_000821.7(GGCX):c.*1725C>A
NM_000821.7(GGCX):c.*1727A>G
NM_000821.7(GGCX):c.*1819A>C rs886056370
NM_000821.7(GGCX):c.*199A>C
NM_000821.7(GGCX):c.*2060T>C rs886056369
NM_000821.7(GGCX):c.*218G>A rs772911409
NM_000821.7(GGCX):c.*2226C>T
NM_000821.7(GGCX):c.*2284C>G rs572084939
NM_000821.7(GGCX):c.*2285T>A rs553827130
NM_000821.7(GGCX):c.*2299C>T rs886056368
NM_000821.7(GGCX):c.*2304T>C rs886056367
NM_000821.7(GGCX):c.*2408T>C rs556052128
NM_000821.7(GGCX):c.*2490T>C
NM_000821.7(GGCX):c.*2560A>G rs886056366
NM_000821.7(GGCX):c.*25T>C rs765806745
NM_000821.7(GGCX):c.*2647T>C rs886056365
NM_000821.7(GGCX):c.*270T>G rs886056377
NM_000821.7(GGCX):c.*2716A>G
NM_000821.7(GGCX):c.*2740A>C
NM_000821.7(GGCX):c.*2774A>G
NM_000821.7(GGCX):c.*285G>A
NM_000821.7(GGCX):c.*2892A>C
NM_000821.7(GGCX):c.*2925G>C rs188039599
NM_000821.7(GGCX):c.*2965C>A
NM_000821.7(GGCX):c.*3000A>G
NM_000821.7(GGCX):c.*309A>G rs886056376
NM_000821.7(GGCX):c.*3177T>G
NM_000821.7(GGCX):c.*3192C>T
NM_000821.7(GGCX):c.*3269A>G
NM_000821.7(GGCX):c.*338T>C
NM_000821.7(GGCX):c.*3393C>T
NM_000821.7(GGCX):c.*3517T>C rs886056364
NM_000821.7(GGCX):c.*3581C>T
NM_000821.7(GGCX):c.*3584C>T
NM_000821.7(GGCX):c.*3630A>T rs886056363
NM_000821.7(GGCX):c.*3647A>G rs541759232
NM_000821.7(GGCX):c.*3703C>T
NM_000821.7(GGCX):c.*3704G>A rs375566923
NM_000821.7(GGCX):c.*3756A>G
NM_000821.7(GGCX):c.*3757T>C rs886056361
NM_000821.7(GGCX):c.*3770T>C
NM_000821.7(GGCX):c.*3841T>A
NM_000821.7(GGCX):c.*3921G>A rs886056360
NM_000821.7(GGCX):c.*3924A>G rs886056359
NM_000821.7(GGCX):c.*3930T>C
NM_000821.7(GGCX):c.*4047T>C rs189391524
NM_000821.7(GGCX):c.*4078G>A
NM_000821.7(GGCX):c.*417G>A
NM_000821.7(GGCX):c.*4195T>G
NM_000821.7(GGCX):c.*4215G>A rs886056358
NM_000821.7(GGCX):c.*4242C>G
NM_000821.7(GGCX):c.*4288G>C rs886056357
NM_000821.7(GGCX):c.*4366C>T
NM_000821.7(GGCX):c.*4397G>A
NM_000821.7(GGCX):c.*4413T>C
NM_000821.7(GGCX):c.*4475T>C
NM_000821.7(GGCX):c.*454C>T
NM_000821.7(GGCX):c.*4562G>A rs113066451
NM_000821.7(GGCX):c.*4681G>A
NM_000821.7(GGCX):c.*469C>T rs557756406
NM_000821.7(GGCX):c.*470G>A rs746348970
NM_000821.7(GGCX):c.*4720G>A
NM_000821.7(GGCX):c.*4744C>T rs886056356
NM_000821.7(GGCX):c.*4798G>A
NM_000821.7(GGCX):c.*4848C>T
NM_000821.7(GGCX):c.*4895T>A rs759788569
NM_000821.7(GGCX):c.*598C>T rs553605433
NM_000821.7(GGCX):c.*610C>T rs532781606
NM_000821.7(GGCX):c.*680G>A rs139300235
NM_000821.7(GGCX):c.*703C>T
NM_000821.7(GGCX):c.*856T>C rs886056374
NM_000821.7(GGCX):c.*91G>T
NM_000821.7(GGCX):c.*973A>G
NM_000821.7(GGCX):c.-23C>T rs537250931
NM_000821.7(GGCX):c.-46C>G
NM_000821.7(GGCX):c.-46C>T rs376371398
NM_000821.7(GGCX):c.-53C>T rs886056381
NM_000821.7(GGCX):c.1008C>T (p.Ala336=)
NM_000821.7(GGCX):c.1046G>C (p.Arg349Pro)
NM_000821.7(GGCX):c.1107C>T (p.Leu369=) rs145056129
NM_000821.7(GGCX):c.1140dup (p.His381fs) rs1558807827
NM_000821.7(GGCX):c.1155+12C>A
NM_000821.7(GGCX):c.1224C>A (p.His408Gln)
NM_000821.7(GGCX):c.1249G>A (p.Asp417Asn)
NM_000821.7(GGCX):c.1299G>C (p.Gln433His)
NM_000821.7(GGCX):c.1355G>C (p.Ser452Thr)
NM_000821.7(GGCX):c.137C>T (p.Ser46Phe) rs201510718
NM_000821.7(GGCX):c.1439+15C>T
NM_000821.7(GGCX):c.1453C>T (p.Arg485Cys)
NM_000821.7(GGCX):c.1455T>C (p.Arg485=)
NM_000821.7(GGCX):c.1485C>T (p.Pro495=)
NM_000821.7(GGCX):c.1492C>T (p.Arg498Cys) rs372161185
NM_000821.7(GGCX):c.159C>A (p.Thr53=) rs61733104
NM_000821.7(GGCX):c.1743G>A (p.Leu581=)
NM_000821.7(GGCX):c.1815C>G (p.Asn605Lys)
NM_000821.7(GGCX):c.1906C>A (p.Pro636Thr) rs61733105
NM_000821.7(GGCX):c.198C>T (p.Val66=) rs147427088
NM_000821.7(GGCX):c.1994G>A (p.Arg665Lys)
NM_000821.7(GGCX):c.2081G>A (p.Arg694His) rs140098905
NM_000821.7(GGCX):c.2119A>C (p.Ile707Leu)
NM_000821.7(GGCX):c.2133T>G (p.Pro711=) rs886056379
NM_000821.7(GGCX):c.2254G>C (p.Asp752His)
NM_000821.7(GGCX):c.24G>A (p.Ala8=) rs371622780
NM_000821.7(GGCX):c.269G>A (p.Arg90Gln)
NM_000821.7(GGCX):c.26G>A (p.Arg9Gln)
NM_000821.7(GGCX):c.271A>C (p.Lys91Gln)
NM_000821.7(GGCX):c.507T>C (p.Phe169=) rs536257863
NM_000821.7(GGCX):c.529A>G (p.Asn177Asp) rs149039591
NM_000821.7(GGCX):c.540-8C>T
NM_000821.7(GGCX):c.57A>T (p.Lys19Asn)
NM_000821.7(GGCX):c.614G>A (p.Gly205Asp)
NM_000821.7(GGCX):c.654G>A (p.Lys218=)
NM_000821.7(GGCX):c.68A>G (p.Glu23Gly) rs886056380
NM_000821.7(GGCX):c.726-4G>T rs146123760
NM_000821.7(GGCX):c.745C>T (p.Leu249=)
NM_000821.7(GGCX):c.789C>T (p.Asp263=) rs146085955
NM_000821.7(GGCX):c.849G>C (p.Val283=) rs149603998
NM_000821.7(GGCX):c.903C>T (p.Tyr301=)
NM_000821.7(GGCX):c.990G>C (p.Leu330=)
NM_000821.7(GGCX):c.994C>A (p.Pro332Thr)

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