List of variants in gene HUWE1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_031407.7(HUWE1):c.12177T>C (p.Gly4059=)	rs426298	0.99420
NM_031407.7(HUWE1):c.2109A>G (p.Ser703=)	rs6638360	0.40138
NM_031407.7(HUWE1):c.6031-4T>A	rs139283158	0.01245
NM_031407.7(HUWE1):c.99A>G (p.Gln33=)	rs61743595	0.01179
NM_031407.7(HUWE1):c.5716+5G>A	rs139135300	0.01175
NM_031407.7(HUWE1):c.10551G>T (p.Leu3517=)	rs61730217	0.00593
NM_031407.7(HUWE1):c.1953C>G (p.Pro651=)	rs139152809	0.00108
NM_031407.7(HUWE1):c.4503C>T (p.Pro1501=)	rs144449744	0.00095
NM_031407.7(HUWE1):c.3082A>G (p.Thr1028Ala)	rs145758265	0.00081
NM_031407.7(HUWE1):c.8298A>G (p.Gln2766=)	rs202214456	0.00053
NM_031407.7(HUWE1):c.10824C>G (p.Leu3608=)	rs191407530	0.00012
NM_031407.7(HUWE1):c.3114C>T (p.Ile1038=)	rs781848587	0.00008
NM_031407.7(HUWE1):c.9486C>T (p.Asn3162=)	rs150660551	0.00008
NM_031407.7(HUWE1):c.5373T>C (p.Tyr1791=)	rs782516736	0.00005
NM_031407.7(HUWE1):c.1470A>G (p.Glu490=)	rs145143264	0.00004
NM_031407.7(HUWE1):c.10038A>G (p.Val3346=)	rs1169705354	0.00003
NM_031407.7(HUWE1):c.4827C>T (p.Tyr1609=)	rs782435043	0.00003
NM_031407.7(HUWE1):c.1000A>G (p.Ile334Val)	rs781928056	0.00002
NM_031407.7(HUWE1):c.10614G>A (p.Thr3538=)	rs138042974	0.00002
NM_031407.7(HUWE1):c.10898C>T (p.Thr3633Ile)	rs781873282	0.00002
NM_031407.7(HUWE1):c.10470A>G (p.Thr3490=)	rs1192210543	0.00001
NM_031407.7(HUWE1):c.4520C>A (p.Thr1507Lys)	rs1382783056	0.00001
NM_031407.7(HUWE1):c.12903= (p.Thr4301=)	rs477171
NM_031407.7(HUWE1):c.9468_9470del (p.Gly3157del)	rs782375893

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