List of variants in gene IGHMBP2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_002180.3(IGHMBP2):c.602T>C (p.Leu201Ser)	rs560096	0.76511
NM_002180.3(IGHMBP2):c.57T>C (p.Leu19=)	rs1249463	0.76080
NM_002180.3(IGHMBP2):c.2011A>G (p.Thr671Ala)	rs622082	0.24183
NM_002180.3(IGHMBP2):c.2316C>T (p.Ser772=)	rs546382	0.24174
NM_002180.3(IGHMBP2):c.2636C>A (p.Thr879Lys)	rs17612126	0.22387
NM_002180.3(IGHMBP2):c.2080C>T (p.Arg694Trp)	rs2236654	0.20662
NM_002180.3(IGHMBP2):c.823A>G (p.Ile275Val)	rs10896380	0.19067
NM_002180.3(IGHMBP2):c.-2C>T	rs4930624	0.18778
NM_002180.3(IGHMBP2):c.1418+18A>G	rs112575423	0.06280
NM_002180.3(IGHMBP2):c.2439G>A (p.Ala813=)	rs624147	0.01079
NM_002180.3(IGHMBP2):c.180C>T (p.Tyr60=)	rs34617762	0.00959
NM_002180.3(IGHMBP2):c.223G>A (p.Ala75Thr)	rs2228206	0.00946
NM_002180.3(IGHMBP2):c.1235+38C>T	rs150602837	0.00863
NM_002180.3(IGHMBP2):c.1757-18C>A	rs77247855	0.00796
NM_002180.3(IGHMBP2):c.2782G>A (p.Glu928Lys)	rs2275996	0.00707
NM_002180.3(IGHMBP2):c.256+9G>A	rs118015540	0.00600
NM_002180.3(IGHMBP2):c.2025C>T (p.Thr675=)	rs138396245	0.00580
NM_002180.3(IGHMBP2):c.741C>T (p.Ala247=)	rs76707931	0.00520
NM_002180.3(IGHMBP2):c.1104C>T (p.Tyr368=)	rs148157556	0.00517
NM_002180.3(IGHMBP2):c.151C>G (p.Gln51Glu)	rs117061430	0.00506
NM_002180.3(IGHMBP2):c.1939G>A (p.Val647Ile)	rs77822399	0.00494
NM_002180.3(IGHMBP2):c.1821C>T (p.His607=)	rs34658653	0.00420
NM_002180.3(IGHMBP2):c.1064C>T (p.Ala355Val)	rs142062146	0.00231
NM_002180.3(IGHMBP2):c.362C>T (p.Ser121Phe)	rs2228205	0.00220
NM_002180.3(IGHMBP2):c.548-10T>G	rs139207271	0.00065
NM_002180.3(IGHMBP2):c.2979G>A (p.Thr993=)	rs201760315	0.00002
NM_002180.3(IGHMBP2):c.2532G>A (p.Ala844=)	rs2228207
NM_002180.3(IGHMBP2):c.726C>G (p.Ala242=)	rs76690064

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