List of variants in gene FANCM reported as benign for not provided

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: 53

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.1581+292C>T	rs226976	0.98000
NM_020937.4(FANCM):c.1582-144C>G	rs10129236	0.22500
NM_020937.4(FANCM):c.1397-58T>G	rs11157433	0.22472
NM_020937.4(FANCM):c.2632G>T (p.Val878Leu)	rs1367580	0.19378
NM_020937.4(FANCM):c.4318-27G>A	rs8020533	0.19361
NM_020937.4(FANCM):c.4516-323T>C	rs10151937	0.19026
NM_020937.4(FANCM):c.2002+141G>A	rs17115860	0.18800
NM_020937.4(FANCM):c.508+76C>T	rs2033385	0.17537
NM_020937.4(FANCM):c.524C>T (p.Ser175Phe)	rs10138997	0.16789
NM_020937.4(FANCM):c.682-166A>G	rs8017844	0.16770
NM_020937.4(FANCM):c.5434C>G (p.Pro1812Ala)	rs3736772	0.08766
NM_020937.4(FANCM):c.1183+205T>C	rs1969713	0.08747
NM_020937.4(FANCM):c.1050+312G>T	rs78571751	0.08587
NM_020937.4(FANCM):c.1582-40A>G	rs78455731	0.08160
NM_020937.4(FANCM):c.1051-304A>G	rs78666636	0.08146
NM_020937.4(FANCM):c.4378A>G (p.Ile1460Val)	rs78211950	0.08024
NM_020937.4(FANCM):c.5340+226A>G	rs17115885	0.05673
NM_020937.4(FANCM):c.*232G>A	rs7155480	0.05342
NM_020937.4(FANCM):c.1788+31del	rs138043605	0.05304
NM_020937.4(FANCM):c.1310-195A>C	rs73340682	0.05166
NM_020937.4(FANCM):c.2160+36C>G	rs78410784	0.04810
NM_020937.4(FANCM):c.4223-100C>T	rs10150209	0.03469
NM_020937.4(FANCM):c.2670T>C (p.Phe890=)	rs8017226	0.03114
NM_020937.4(FANCM):c.919-281G>A	rs77415294	0.03098
NM_020937.4(FANCM):c.6141T>C (p.Asp2047=)	rs8018014	0.03012
NM_020937.4(FANCM):c.4516-163T>C	rs115592240	0.03004
NM_020937.4(FANCM):c.919-293A>G	rs76768362	0.03004
NM_020937.4(FANCM):c.1396+26G>A	rs17635457	0.02255
NM_020937.4(FANCM):c.2003-256C>G	rs11851069	0.01926
NM_020937.4(FANCM):c.5341-63G>A	rs78876918	0.01905
NM_020937.4(FANCM):c.624A>G (p.Ile208Met)	rs45547534	0.01077
NM_020937.4(FANCM):c.5224A>G (p.Ile1742Val)	rs143662421	0.00824
NM_020937.4(FANCM):c.2190A>G (p.Gln730=)	rs117392855	0.00320
NM_020937.4(FANCM):c.5808C>T (p.Ser1936=)	rs142333130	0.00178
NM_020937.4(FANCM):c.30G>A (p.Gln10=)	rs145745979	0.00014
NM_020937.4(FANCM):c.1183+8A>G	rs538172189	0.00001
GRCh37/hg19 14q21.2(chr14:45611090-45612490)x1
GRCh37/hg19 14q21.2(chr14:45611090-45619217)x1
NM_020937.4(FANCM):c.1184-281del	rs5808292
NM_020937.4(FANCM):c.1184-281dup	rs5808292
NM_020937.4(FANCM):c.1310-36dup	rs147550893
NM_020937.4(FANCM):c.1396+279G>A	rs45607635
NM_020937.4(FANCM):c.1397-15TA[6]	rs112326758
NM_020937.4(FANCM):c.1789-154dup	rs781175707
NM_020937.4(FANCM):c.1789-155_1789-154dup	rs781175707
NM_020937.4(FANCM):c.4223-234A>T	rs114245176
NM_020937.4(FANCM):c.4387-39A>T	rs145077997
NM_020937.4(FANCM):c.4516-262del	rs1176189406
NM_020937.4(FANCM):c.4516-5_4516-2del	rs796584585
NM_020937.4(FANCM):c.759+205=	rs170542
NM_020937.4(FANCM):c.876G>T (p.Pro292=)	rs150757891
NM_020937.4(FANCM):c.918+291CA[11]	rs147489712
NM_020937.4(FANCM):c.918+291CA[13]	rs147489712

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