ClinVar Miner

List of variants in gene FANCM reported as benign for Fanconi anemia complementation group A

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_020937.3(FANCM):c.4516-5_4516-2delCTTA rs796584585
NM_020937.4(FANCM):c.1041G>A (p.Pro347=) rs140998495
NM_020937.4(FANCM):c.1964A>G (p.Asn655Ser) rs61753893
NM_020937.4(FANCM):c.2190A>G (p.Gln730=) rs117392855
NM_020937.4(FANCM):c.229A>G (p.Thr77Ala) rs61746895
NM_020937.4(FANCM):c.2445G>A (p.Ser815=) rs61745871
NM_020937.4(FANCM):c.2632G>T (p.Val878Leu) rs1367580
NM_020937.4(FANCM):c.2670T>C (p.Phe890=) rs8017226
NM_020937.4(FANCM):c.2749A>G (p.Ile917Val) rs148871932
NM_020937.4(FANCM):c.3040G>T (p.Gly1014Cys) rs77532752
NM_020937.4(FANCM):c.30G>A (p.Gln10=) rs145745979
NM_020937.4(FANCM):c.3547T>C (p.Leu1183=) rs142667852
NM_020937.4(FANCM):c.3758A>G (p.Asn1253Ser) rs45604036
NM_020937.4(FANCM):c.3863A>G (p.Asn1288Ser) rs116519044
NM_020937.4(FANCM):c.3920A>G (p.Tyr1307Cys) rs61730251
NM_020937.4(FANCM):c.4222+7T>G rs148675704
NM_020937.4(FANCM):c.4260C>T (p.Asp1420=) rs113819179
NM_020937.4(FANCM):c.4563A>C (p.Glu1521Asp) rs113986680
NM_020937.4(FANCM):c.4799C>T (p.Thr1600Ile) rs61746943
NM_020937.4(FANCM):c.4931G>A (p.Arg1644Gln) rs138151018
NM_020937.4(FANCM):c.5142G>A (p.Ala1714=) rs111894696
NM_020937.4(FANCM):c.5190G>A (p.Gln1730=) rs7142192
NM_020937.4(FANCM):c.5224A>G (p.Ile1742Val) rs143662421
NM_020937.4(FANCM):c.524C>T (p.Ser175Phe) rs10138997
NM_020937.4(FANCM):c.527C>T (p.Thr176Ile) rs77374493
NM_020937.4(FANCM):c.5577T>C (p.Asn1859=) rs113831595
NM_020937.4(FANCM):c.5627A>G (p.Asn1876Ser) rs45557033
NM_020937.4(FANCM):c.5656C>T (p.His1886Tyr) rs79343837
NM_020937.4(FANCM):c.5808C>T (p.Ser1936=) rs142333130
NM_020937.4(FANCM):c.6141T>C (p.Asp2047=) rs8018014
NM_020937.4(FANCM):c.624A>G (p.Ile208Met) rs45547534
NM_020937.4(FANCM):c.990A>G (p.Thr330=) rs138677111

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