ClinVar Miner

List of variants in gene HCFC1 reported as uncertain significance for not specified

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Total variants: 17
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HGVS dbSNP
NM_005334.3(HCFC1):c.1084+8C>T rs367698803
NM_005334.3(HCFC1):c.1214C>T (p.Thr405Met) rs782047045
NM_005334.3(HCFC1):c.1472G>T (p.Gly491Val) rs1057524819
NM_005334.3(HCFC1):c.2463T>A (p.Ile821=) rs371411952
NM_005334.3(HCFC1):c.2691G>A (p.Ala897=) rs374223163
NM_005334.3(HCFC1):c.3126G>A (p.Gln1042=) rs782501125
NM_005334.3(HCFC1):c.3492C>T (p.Ser1164=) rs376049260
NM_005334.3(HCFC1):c.3690G>A (p.Ala1230=) rs782484757
NM_005334.3(HCFC1):c.3846G>A (p.Ser1282=) rs372301724
NM_005334.3(HCFC1):c.4475C>G (p.Pro1492Arg) rs782407440
NM_005334.3(HCFC1):c.4576G>A (p.Ala1526Thr) rs782652831
NM_005334.3(HCFC1):c.4594G>A (p.Ala1532Thr) rs782665288
NM_005334.3(HCFC1):c.4619C>T (p.Thr1540Ile) rs781788935
NM_005334.3(HCFC1):c.4722A>C (p.Pro1574=) rs1557112957
NM_005334.3(HCFC1):c.5528G>C (p.Gly1843Ala) rs797045609
NM_005334.3(HCFC1):c.905-3C>T rs200367055
NM_005334.3(HCFC1):c.984C>T (p.Val328=) rs782409511

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