List of variants in gene FANCA reported as benign by PreventionGenetics, part of Exact Sciences

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: 38

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.710-12A>G	rs1800286	0.71452
NM_000135.4(FANCA):c.1084-49G>C	rs1800287	0.53385
NM_000135.4(FANCA):c.796A>G (p.Thr266Ala)	rs7190823	0.52564
NM_000135.4(FANCA):c.1501G>A (p.Gly501Ser)	rs2239359	0.51262
NM_000135.4(FANCA):c.1826+15T>C	rs1800337	0.51138
NM_000135.4(FANCA):c.2426G>A (p.Gly809Asp)	rs7195066	0.46389
NM_000135.4(FANCA):c.1226-20A>G	rs1800330	0.41702
NM_000135.4(FANCA):c.3240-42G>A	rs1800345	0.40844
NM_000135.4(FANCA):c.2151+8T>C	rs1800340	0.40536
NM_000135.4(FANCA):c.1084-29A>G	rs6500452	0.39672
NM_000135.4(FANCA):c.3654A>G (p.Pro1218=)	rs1800358	0.12784
NM_000135.4(FANCA):c.2602-36G>T	rs2159116	0.11784
NM_000135.4(FANCA):c.1143G>T (p.Thr381=)	rs1800331	0.06866
NM_000135.4(FANCA):c.894-8A>G	rs11648881	0.06110
NM_000135.4(FANCA):c.1927C>G (p.Pro643Ala)	rs17232910	0.05919
NM_000135.4(FANCA):c.1777-29T>C	rs2302162	0.05904
NM_000135.4(FANCA):c.2779-7T>C	rs17233253	0.05872
NM_000135.4(FANCA):c.2901C>T (p.Ser967=)	rs17226980	0.05869
NM_000135.4(FANCA):c.3067-4T>C	rs17227064	0.05860
NM_000135.4(FANCA):c.3067-23G>A	rs17227057	0.05859
NM_000135.4(FANCA):c.3765+37G>A	rs34420680	0.05858
NM_000135.4(FANCA):c.2602-46T>A	rs11076620	0.05847
NM_000135.4(FANCA):c.1235C>T (p.Ala412Val)	rs11646374	0.05837
NM_000135.4(FANCA):c.3263C>T (p.Ser1088Phe)	rs17233497	0.05303
NM_000135.4(FANCA):c.427-25T>A	rs9282685	0.05123
NM_000135.4(FANCA):c.542C>T (p.Ala181Val)	rs17232246	0.04972
NM_000135.4(FANCA):c.1941G>A (p.Glu647=)	rs17232917	0.03300
NM_000135.4(FANCA):c.3348+18A>G	rs1800347	0.02828
NM_000135.4(FANCA):c.2151G>T (p.Met717Ile)	rs1131660	0.02234
NM_000135.4(FANCA):c.755A>G (p.Asp252Gly)	rs17225943	0.01851
NM_000135.4(FANCA):c.1627-32T>C	rs17226337	0.01179
NM_000135.4(FANCA):c.932T>C (p.Ile311Thr)	rs75501942	0.00334
NM_000135.4(FANCA):c.623C>T (p.Ser208Leu)	rs144420697	0.00325
NM_000135.4(FANCA):c.2021C>T (p.Ser674Leu)	rs17232973	0.00257
NM_000135.4(FANCA):c.1290G>A (p.Ala430=)	rs1800332
NM_000135.4(FANCA):c.1777-41_1777-38del	rs56163653
NM_000135.4(FANCA):c.1826+30_1826+31insTG	rs36204974
NM_000135.4(FANCA):c.710-142_710-141dup	rs17232344

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.