ClinVar Miner

List of variants in gene HCFC1 reported as likely benign by Invitae

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Total variants: 42
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HGVS dbSNP
NM_005334.3(HCFC1):c.1122C>T (p.Arg374=) rs781840891
NM_005334.3(HCFC1):c.1698G>A (p.Thr566=)
NM_005334.3(HCFC1):c.1803+7G>A
NM_005334.3(HCFC1):c.1842C>T (p.Ala614=)
NM_005334.3(HCFC1):c.1980C>T (p.Thr660=)
NM_005334.3(HCFC1):c.2232G>A (p.Ala744=) rs1557115422
NM_005334.3(HCFC1):c.2316C>T (p.Ile772=)
NM_005334.3(HCFC1):c.2346C>T (p.Gly782=)
NM_005334.3(HCFC1):c.237C>A (p.Pro79=)
NM_005334.3(HCFC1):c.2436G>A (p.Ala812=)
NM_005334.3(HCFC1):c.2566C>T (p.Leu856=)
NM_005334.3(HCFC1):c.2817A>T (p.Thr939=) rs782349400
NM_005334.3(HCFC1):c.2872A>G (p.Thr958Ala) rs3027884
NM_005334.3(HCFC1):c.2973C>T (p.Thr991=)
NM_005334.3(HCFC1):c.3103G>C (p.Ala1035Pro)
NM_005334.3(HCFC1):c.3180G>T (p.Val1060=)
NM_005334.3(HCFC1):c.3255G>A (p.Thr1085=) rs782017804
NM_005334.3(HCFC1):c.3279C>T (p.Thr1093=)
NM_005334.3(HCFC1):c.333C>T (p.Tyr111=)
NM_005334.3(HCFC1):c.3459T>C (p.Thr1153=)
NM_005334.3(HCFC1):c.3579T>C (p.Leu1193=)
NM_005334.3(HCFC1):c.3903C>T (p.Thr1301=) rs375212345
NM_005334.3(HCFC1):c.3951C>T (p.Cys1317=)
NM_005334.3(HCFC1):c.4125C>T (p.Ala1375=)
NM_005334.3(HCFC1):c.4158C>T (p.Thr1386=)
NM_005334.3(HCFC1):c.4159G>A (p.Val1387Met) rs200164926
NM_005334.3(HCFC1):c.4182G>A (p.Ala1394=) rs782820533
NM_005334.3(HCFC1):c.4218G>A (p.Ala1406=) rs782670703
NM_005334.3(HCFC1):c.4245G>A (p.Arg1415=)
NM_005334.3(HCFC1):c.4260C>G (p.Pro1420=)
NM_005334.3(HCFC1):c.4263C>A (p.Pro1421=)
NM_005334.3(HCFC1):c.4266T>C (p.Cys1422=)
NM_005334.3(HCFC1):c.4773A>G (p.Leu1591=)
NM_005334.3(HCFC1):c.504-9C>T
NM_005334.3(HCFC1):c.5397C>A (p.Pro1799=)
NM_005334.3(HCFC1):c.5613C>T (p.Ala1871=)
NM_005334.3(HCFC1):c.5769C>T (p.Tyr1923=)
NM_005334.3(HCFC1):c.5784C>T (p.Ala1928=)
NM_005334.3(HCFC1):c.579C>T (p.Tyr193=)
NM_005334.3(HCFC1):c.6042C>T (p.Asn2014=) rs199953428
NM_005334.3(HCFC1):c.6069-4C>T
NM_005334.3(HCFC1):c.648C>G (p.Ser216=)

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