ClinVar Miner

List of variants in gene FANCA reported as benign by PreventionGenetics

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Total variants: 38
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HGVS dbSNP
NM_000135.2(FANCA):c.1777-41_1777-38delTTTC rs56163653
NM_000135.4(FANCA):c.1084-29A>G rs6500452
NM_000135.4(FANCA):c.1084-49G>C rs1800287
NM_000135.4(FANCA):c.1143G>T (p.Thr381=) rs1800331
NM_000135.4(FANCA):c.1226-20A>G rs1800330
NM_000135.4(FANCA):c.1235C>T (p.Ala412Val) rs11646374
NM_000135.4(FANCA):c.1290G>A (p.Ala430=) rs1800332
NM_000135.4(FANCA):c.1501G>A (p.Gly501Ser) rs2239359
NM_000135.4(FANCA):c.1627-32T>C rs17226337
NM_000135.4(FANCA):c.1777-29T>C rs2302162
NM_000135.4(FANCA):c.1826+15T>C rs1800337
NM_000135.4(FANCA):c.1826+30_1826+31insTG rs36204974
NM_000135.4(FANCA):c.1927C>G (p.Pro643Ala) rs17232910
NM_000135.4(FANCA):c.1941G>A (p.Glu647=) rs17232917
NM_000135.4(FANCA):c.2151+8T>C rs1800340
NM_000135.4(FANCA):c.2151G>T (p.Met717Ile) rs1131660
NM_000135.4(FANCA):c.2426G>A (p.Gly809Asp) rs7195066
NM_000135.4(FANCA):c.2602-36G>T rs2159116
NM_000135.4(FANCA):c.2602-46T>A rs11076620
NM_000135.4(FANCA):c.2779-7T>C rs17233253
NM_000135.4(FANCA):c.2901C>T (p.Ser967=) rs17226980
NM_000135.4(FANCA):c.3067-23G>A rs17227057
NM_000135.4(FANCA):c.3067-4T>C rs17227064
NM_000135.4(FANCA):c.3240-42G>A rs1800345
NM_000135.4(FANCA):c.3263C>T (p.Ser1088Phe) rs17233497
NM_000135.4(FANCA):c.3348+18A>G rs1800347
NM_000135.4(FANCA):c.3408+33T>C rs17227191
NM_000135.4(FANCA):c.3408+45G>A rs1800355
NM_000135.4(FANCA):c.3654A>G (p.Pro1218=) rs1800358
NM_000135.4(FANCA):c.3765+37G>A rs34420680
NM_000135.4(FANCA):c.427-25T>A rs9282685
NM_000135.4(FANCA):c.542C>T (p.Ala181Val) rs17232246
NM_000135.4(FANCA):c.623C>T (p.Ser208Leu) rs144420697
NM_000135.4(FANCA):c.710-12A>G rs1800286
NM_000135.4(FANCA):c.755A>G (p.Asp252Gly) rs17225943
NM_000135.4(FANCA):c.796A>G (p.Thr266Ala) rs7190823
NM_000135.4(FANCA):c.894-8A>G rs11648881
NM_000135.4(FANCA):c.932T>C (p.Ile311Thr) rs75501942

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