List of variants in gene NEXMIF reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.2139G>A (p.Glu713=)	rs139194076	0.00055
NM_001008537.3(NEXMIF):c.4509T>C (p.Pro1503=)	rs41303725	0.00055
NM_001008537.3(NEXMIF):c.133G>A (p.Ala45Thr)	rs199960807	0.00030
NM_001008537.3(NEXMIF):c.4320C>T (p.Asn1440=)	rs769979162	0.00027
NM_001008537.3(NEXMIF):c.4048G>A (p.Asp1350Asn)	rs200982385	0.00017
NM_001008537.3(NEXMIF):c.2315G>A (p.Arg772His)	rs142822527	0.00015
NM_001008537.3(NEXMIF):c.42C>T (p.Asn14=)	rs370708043	0.00013
NM_001008537.3(NEXMIF):c.3823A>G (p.Ser1275Gly)	rs201434271	0.00012
NM_001008537.3(NEXMIF):c.3402C>A (p.His1134Gln)	rs138632224	0.00011
NM_001008537.3(NEXMIF):c.1983C>T (p.His661=)	rs138583612	0.00010
NM_001008537.3(NEXMIF):c.3812T>C (p.Met1271Thr)	rs138236888	0.00010
NM_001008537.3(NEXMIF):c.4422G>A (p.Lys1474=)	rs371190782	0.00009
NM_001008537.3(NEXMIF):c.4065C>T (p.Tyr1355=)	rs755840617	0.00008
NM_001008537.3(NEXMIF):c.1415C>G (p.Ser472Cys)	rs770738202	0.00006
NM_001008537.3(NEXMIF):c.4235G>A (p.Arg1412His)	rs374045534	0.00006
NM_001008537.3(NEXMIF):c.262G>A (p.Glu88Lys)	rs927047621	0.00004
NM_001008537.3(NEXMIF):c.153G>A (p.Pro51=)	rs147096194	0.00003
NM_001008537.3(NEXMIF):c.4326G>A (p.Pro1442=)	rs141163613	0.00003
NM_001008537.3(NEXMIF):c.1418C>T (p.Ser473Phe)	rs1305966854	0.00002
NM_001008537.3(NEXMIF):c.3222G>A (p.Pro1074=)	rs748567167	0.00001
NM_001008537.3(NEXMIF):c.653G>A (p.Arg218Gln)	rs747496798	0.00001
NM_001008537.3(NEXMIF):c.690G>A (p.Pro230=)	rs776754896	0.00001
NM_001008537.3(NEXMIF):c.1410C>T (p.Gly470=)
NM_001008537.3(NEXMIF):c.1575C>T (p.Pro525=)
NM_001008537.3(NEXMIF):c.2087G>T (p.Gly696Val)
NM_001008537.3(NEXMIF):c.2373A>G (p.Thr791=)	rs61742545
NM_001008537.3(NEXMIF):c.2439G>T (p.Gly813=)
NM_001008537.3(NEXMIF):c.339A>G (p.Ser113=)
NM_001008537.3(NEXMIF):c.3429T>C (p.Asp1143=)
NM_001008537.3(NEXMIF):c.3867C>T (p.Ser1289=)
NM_001008537.3(NEXMIF):c.4012A>G (p.Ile1338Val)
NM_001008537.3(NEXMIF):c.4049del (p.Asp1350fs)	rs2147439030
NM_001008537.3(NEXMIF):c.4108T>C (p.Leu1370=)	rs2080098614
NM_001008537.3(NEXMIF):c.4284T>C (p.Asp1428=)

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