List of variants in gene IGHMBP2 reported as benign by Illumina Laboratory Services, Illumina

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_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.*255T>C	rs564244	0.75917
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.*681T>C	rs9095	0.22873
NM_002180.3(IGHMBP2):c.2636C>A (p.Thr879Lys)	rs17612126	0.22387
NM_002180.3(IGHMBP2):c.*427C>T	rs3750980	0.22234
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.*665C>T	rs9769	0.14339
NM_002180.2(IGHMBP2):c.-68T>C	rs57258566	0.01836
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.*22C>T	rs80298715	0.00795
NM_002180.3(IGHMBP2):c.2782G>A (p.Glu928Lys)	rs2275996	0.00707
NM_002180.3(IGHMBP2):c.*744G>A	rs116625875	0.00591
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.-28C>A	rs117368938	0.00135
NM_002180.3(IGHMBP2):c.2322A>G (p.Glu774=)	rs11228414	0.00085
NM_002180.3(IGHMBP2):c.548-10T>G	rs139207271	0.00065
NM_002180.3(IGHMBP2):c.344C>T (p.Thr115Met)	rs181657861	0.00046
NM_002180.3(IGHMBP2):c.366C>T (p.His122=)	rs144401213	0.00019
NM_002180.3(IGHMBP2):c.1827G>A (p.Ala609=)	rs541245852	0.00003
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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