List of variants in gene FANCM reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.5808C>T (p.Ser1936=)	rs142333130	0.00178
NM_020937.4(FANCM):c.1551G>A (p.Thr517=)	rs139535827	0.00047
NM_020937.4(FANCM):c.159C>T (p.Asp53=)	rs147559750	0.00046
NM_020937.4(FANCM):c.5205G>A (p.Ser1735=)	rs138090463	0.00020
NM_020937.4(FANCM):c.5341-19G>A	rs375732305	0.00014
NM_020937.4(FANCM):c.1668T>C (p.Asp556=)	rs142380037	0.00009
NM_020937.4(FANCM):c.3735A>T (p.Ile1245=)	rs574509639	0.00008
NM_020937.4(FANCM):c.4222+18dup	rs760075544	0.00008
NM_020937.4(FANCM):c.1397-16T>A	rs752547104	0.00006
NM_020937.4(FANCM):c.3096T>C (p.Asp1032=)	rs199507375	0.00006
NM_020937.4(FANCM):c.1752G>A (p.Arg584=)	rs373696744	0.00004
NM_020937.4(FANCM):c.231C>T (p.Thr77=)	rs377164876	0.00004
NM_020937.4(FANCM):c.3882T>C (p.Val1294=)	rs774984454	0.00004
NM_020937.4(FANCM):c.4578T>G (p.Val1526=)	rs368982372	0.00003
NM_020937.4(FANCM):c.6060G>A (p.Glu2020=)	rs949619907	0.00003
NM_020937.4(FANCM):c.6084T>C (p.Tyr2028=)	rs756119280	0.00003
NM_020937.4(FANCM):c.3513T>C (p.Pro1171=)	rs771150480	0.00002
NM_020937.4(FANCM):c.1184-20C>A	rs763504552	0.00001
NM_020937.4(FANCM):c.1530C>T (p.Gly510=)	rs367951081	0.00001
NM_020937.4(FANCM):c.2721T>G (p.Ala907=)	rs150172333	0.00001
NM_020937.4(FANCM):c.366C>G (p.Ala122=)	rs770311755	0.00001
NM_020937.4(FANCM):c.3837A>G (p.Ala1279=)	rs188061266	0.00001
NM_020937.4(FANCM):c.3888C>A (p.Ile1296=)	rs764040527	0.00001
NM_020937.4(FANCM):c.4515+14del	rs747887646
NM_020937.4(FANCM):c.4686A>G (p.Arg1562=)	rs1889498706
NM_020937.4(FANCM):c.4780-4G>C	rs1486453187
NM_020937.4(FANCM):c.480C>T (p.Ile160=)	rs753171718
NM_020937.4(FANCM):c.682-7del	rs759364320
NM_020937.4(FANCM):c.876G>A (p.Pro292=)	rs150757891

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