List of variants in gene NEB reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 41

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.4649A>G (p.Lys1550Arg)	rs114089598	0.00312
NM_001164508.2(NEB):c.7126G>C (p.Val2376Leu)	rs141155976	0.00142
NM_001164508.2(NEB):c.3623T>C (p.Ile1208Thr)	rs201141958	0.00137
NM_001164508.2(NEB):c.17510A>G (p.Lys5837Arg)	rs201962649	0.00114
NM_001164508.2(NEB):c.4834C>T (p.Arg1612Cys)	rs200545007	0.00108
NM_001164508.2(NEB):c.3986A>C (p.Asp1329Ala)	rs115986826	0.00095
NM_001164508.2(NEB):c.19219G>A (p.Glu6407Lys)	rs144539316	0.00078
NM_001164508.2(NEB):c.5503C>T (p.Arg1835Trp)	rs199694315	0.00039
NM_001164508.2(NEB):c.20162T>C (p.Leu6721Pro)	rs111517514	0.00029
NM_001164508.2(NEB):c.20212G>A (p.Asp6738Asn)	rs201337732	0.00011
NM_001164508.2(NEB):c.21056G>A (p.Arg7019His)	rs377443184	0.00011
NM_001164508.2(NEB):c.9620G>A (p.Arg3207His)	rs111841612	0.00011
NM_001164508.2(NEB):c.9854G>A (p.Arg3285His)	rs376932516	0.00011
NM_001164508.2(NEB):c.11077C>T (p.Arg3693Cys)	rs539139958	0.00009
NM_001164508.2(NEB):c.355A>G (p.Thr119Ala)	rs182207224	0.00008
NM_001164508.2(NEB):c.11717G>A (p.Arg3906His)	rs556930902	0.00006
NM_001164508.2(NEB):c.20441G>A (p.Arg6814His)	rs773584363	0.00006
NM_001164508.2(NEB):c.8063A>G (p.His2688Arg)	rs201119402	0.00006
NM_001164508.2(NEB):c.3716G>T (p.Ser1239Ile)	rs201541240	0.00005
NM_001164508.2(NEB):c.19989A>T (p.Arg6663Ser)	rs755153044	0.00004
NM_001164508.2(NEB):c.17129A>G (p.Lys5710Arg)	rs200501968	0.00003
NM_001164508.2(NEB):c.6449C>T (p.Ala2150Val)	rs375256600	0.00003
NM_001164508.2(NEB):c.11762C>T (p.Pro3921Leu)	rs371675358	0.00001
NM_001164508.2(NEB):c.19313A>G (p.His6438Arg)	rs1015281617	0.00001
NM_001164508.2(NEB):c.4877A>G (p.His1626Arg)	rs1374856817	0.00001
NM_001164508.2(NEB):c.7378C>T (p.Pro2460Ser)	rs1360504212	0.00001
NM_001164508.2(NEB):c.7547G>A (p.Arg2516Gln)	rs753647278	0.00001
NM_001164508.2(NEB):c.7628G>A (p.Arg2543Gln)	rs758589097	0.00001
NM_001164508.2(NEB):c.10231_10233delinsACC (p.Ala3411Thr)	rs2154058279
NM_001164508.2(NEB):c.11755G>T (p.Asp3919Tyr)	rs201483656
NM_001164508.2(NEB):c.1316A>G (p.Glu439Gly)	rs1553608272
NM_001164508.2(NEB):c.17546G>A (p.Arg5849His)
NM_001164508.2(NEB):c.19285_19286delinsAA (p.Ala6429Asn)	rs796065338
NM_001164508.2(NEB):c.19371T>G (p.Ser6457Arg)
NM_001164508.2(NEB):c.20711A>G (p.Glu6904Gly)	rs886054930
NM_001164508.2(NEB):c.3740T>A (p.Val1247Asp)	rs753696014
NM_001164508.2(NEB):c.4252G>A (p.Ala1418Thr)	rs1444597977
NM_001164508.2(NEB):c.5086A>G (p.Ile1696Val)
NM_001164508.2(NEB):c.5932A>G (p.Met1978Val)
NM_001164508.2(NEB):c.6254C>T (p.Pro2085Leu)	rs773025267
NM_001164508.2(NEB):c.707C>G (p.Ala236Gly)	rs2099780369

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