List of variants in gene FANCC reported as uncertain significance by Natera, Inc.

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 61

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.178G>A (p.Val60Ile)	rs138629441	0.00091
NM_000136.3(FANCC):c.248A>G (p.Tyr83Cys)	rs140992397	0.00007
NM_000136.3(FANCC):c.202G>C (p.Gly68Arg)	rs777111154	0.00004
NM_000136.3(FANCC):c.28T>G (p.Cys10Gly)	rs147479204	0.00004
NM_000136.3(FANCC):c.9A>T (p.Gln3His)	rs769585639	0.00004
NM_000136.3(FANCC):c.127G>A (p.Glu43Lys)	rs374836770	0.00003
NM_000136.3(FANCC):c.146A>G (p.Tyr49Cys)	rs761845692	0.00003
NM_000136.3(FANCC):c.191T>G (p.Phe64Cys)	rs375921240	0.00003
NM_000136.3(FANCC):c.338G>C (p.Trp113Ser)	rs1064793405	0.00003
NM_000136.3(FANCC):c.46A>T (p.Met16Leu)	rs1390412870	0.00003
NM_000136.3(FANCC):c.521G>A (p.Arg174Gln)	rs755283850	0.00003
NM_000136.3(FANCC):c.233C>A (p.Pro78His)	rs138722298	0.00002
NM_000136.3(FANCC):c.349G>A (p.Val117Ile)	rs781167993	0.00002
NM_000136.3(FANCC):c.473C>T (p.Ala158Val)	rs776429990	0.00002
NM_000136.3(FANCC):c.-2A>G	rs773045474	0.00001
NM_000136.3(FANCC):c.104G>C (p.Cys35Ser)	rs143212932	0.00001
NM_000136.3(FANCC):c.109C>G (p.His37Asp)	rs864622230	0.00001
NM_000136.3(FANCC):c.112G>A (p.Val38Met)	rs778951584	0.00001
NM_000136.3(FANCC):c.160G>A (p.Glu54Lys)	rs1564794487	0.00001
NM_000136.3(FANCC):c.176C>T (p.Thr59Ile)	rs149566909	0.00001
NM_000136.3(FANCC):c.238A>G (p.Ile80Val)	rs1064793110	0.00001
NM_000136.3(FANCC):c.239T>C (p.Ile80Thr)	rs4647419	0.00001
NM_000136.3(FANCC):c.262A>C (p.Lys88Gln)	rs1060502519	0.00001
NM_000136.3(FANCC):c.271A>G (p.Ile91Val)	rs771619614	0.00001
NM_000136.3(FANCC):c.278G>A (p.Cys93Tyr)	rs774029807	0.00001
NM_000136.3(FANCC):c.329T>C (p.Leu110Pro)	rs777731560	0.00001
NM_000136.3(FANCC):c.347G>A (p.Gly116Asp)	rs1282106098	0.00001
NM_000136.3(FANCC):c.364C>T (p.Leu122Phe)	rs1064796148	0.00001
NM_000136.3(FANCC):c.397C>T (p.Leu133Phe)	rs587779906	0.00001
NM_000136.3(FANCC):c.436_438del (p.Tyr146del)	rs761347179	0.00001
NM_000136.3(FANCC):c.440C>T (p.Pro147Leu)	rs730881711	0.00001
NM_000136.3(FANCC):c.46A>G (p.Met16Val)	rs1390412870	0.00001
NM_000136.3(FANCC):c.472G>C (p.Ala158Pro)	rs372338418	0.00001
NM_000136.3(FANCC):c.476C>T (p.Ser159Phe)	rs1588218581	0.00001
NM_000136.3(FANCC):c.521+5G>C	rs1301899973	0.00001
NM_000136.3(FANCC):c.8A>C (p.Gln3Pro)	rs1415268424	0.00001
NM_000136.3(FANCC):c.110A>C (p.His37Pro)	rs1564794663
NM_000136.3(FANCC):c.120G>C (p.Gln40His)	rs905858585
NM_000136.3(FANCC):c.140A>G (p.Lys47Arg)	rs1588353368
NM_000136.3(FANCC):c.156G>C (p.Leu52Phe)	rs1060502518
NM_000136.3(FANCC):c.166-3C>T	rs1554857868
NM_000136.3(FANCC):c.17T>G (p.Val6Gly)	rs527289778
NM_000136.3(FANCC):c.197C>T (p.Thr66Ile)	rs762234072
NM_000136.3(FANCC):c.214G>A (p.Ala72Thr)	rs567465885
NM_000136.3(FANCC):c.228G>T (p.Trp76Cys)	rs876661132
NM_000136.3(FANCC):c.23T>C (p.Leu8Pro)	rs752249253
NM_000136.3(FANCC):c.266T>G (p.Ile89Ser)	rs2136049598
NM_000136.3(FANCC):c.340A>T (p.Ile114Leu)	rs1830580247
NM_000136.3(FANCC):c.349_360del (p.Val117_His120del)	rs1825723799
NM_000136.3(FANCC):c.35A>G (p.Tyr12Cys)	rs762884109
NM_000136.3(FANCC):c.371C>T (p.Ala124Val)	rs374602991
NM_000136.3(FANCC):c.390A>T (p.Glu130Asp)	rs1419677503
NM_000136.3(FANCC):c.413T>G (p.Leu138Arg)	rs1564720454
NM_000136.3(FANCC):c.424C>G (p.Pro142Ala)	rs864622581
NM_000136.3(FANCC):c.425C>A (p.Pro142His)	rs1064793605
NM_000136.3(FANCC):c.439C>A (p.Pro147Thr)	rs1564720334
NM_000136.3(FANCC):c.491A>T (p.Asn164Ile)	rs950623649
NM_000136.3(FANCC):c.509A>G (p.Asn170Ser)	rs749322338
NM_000136.3(FANCC):c.511A>G (p.Thr171Ala)	rs1554842592
NM_000136.3(FANCC):c.516A>G (p.Gln172=)	rs748322179
NM_000136.3(FANCC):c.61G>C (p.Val21Leu)	rs772386467

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