List of variants in gene CNTNAP2 reported as likely 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: 32

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HGVS	dbSNP	gnomAD frequency
NM_014141.6(CNTNAP2):c.2256-6A>T	rs10240482	0.10641
NM_014141.6(CNTNAP2):c.2099-15T>C	rs75858942	0.04429
NM_014141.6(CNTNAP2):c.*3531G>A	rs79360609	0.04371
NM_014141.6(CNTNAP2):c.1710G>A (p.Ser570=)	rs2286128	0.03626
NM_014141.6(CNTNAP2):c.*3392C>T	rs115420302	0.02775
NM_014141.6(CNTNAP2):c.*3540G>A	rs114585910	0.02773
NM_014141.6(CNTNAP2):c.*2151A>G	rs28369221	0.02742
NM_014141.6(CNTNAP2):c.3476-15C>A	rs77706740	0.02606
NM_014141.6(CNTNAP2):c.*2875dup	rs138367128	0.02522
NM_014141.6(CNTNAP2):c.*1017T>G	rs77001133	0.02487
NM_014141.6(CNTNAP2):c.3797-6C>T	rs79777576	0.01899
NM_014141.6(CNTNAP2):c.*3921G>A	rs141005348	0.01856
NM_014141.6(CNTNAP2):c.*2665C>T	rs7791181	0.01854
NM_014141.6(CNTNAP2):c.318C>T (p.Ser106=)	rs61732853	0.01773
NM_014141.6(CNTNAP2):c.*48G>A	rs78018010	0.01715
NM_014141.6(CNTNAP2):c.*1433A>G	rs78484397	0.01362
NM_014141.6(CNTNAP2):c.1854C>T (p.Gly618=)	rs61732849	0.01075
NM_014141.6(CNTNAP2):c.*4071G>A	rs147886818	0.00288
NM_014141.6(CNTNAP2):c.*3433G>A	rs142623983	0.00279
NM_014141.6(CNTNAP2):c.3105C>T (p.Asn1035=)	rs112483670	0.00264
NM_014141.6(CNTNAP2):c.1220A>G (p.Asn407Ser)	rs143877693	0.00253
NM_014141.6(CNTNAP2):c.681C>T (p.His227=)	rs142984073	0.00236
NM_014141.6(CNTNAP2):c.*3796C>T	rs183556756	0.00053
NM_014141.6(CNTNAP2):c.2190C>T (p.Cys730=)	rs74354654	0.00029
NM_014141.6(CNTNAP2):c.*1482A>T	rs186254614	0.00018
NM_014141.6(CNTNAP2):c.515T>C (p.Ile172Thr)	rs201326295	0.00017
NM_014141.6(CNTNAP2):c.341G>A (p.Arg114Gln)	rs189731792	0.00005
NM_014141.6(CNTNAP2):c.3716-6C>G	rs77025884	0.00004
NM_014141.6(CNTNAP2):c.1276_1280dup	rs369615005
NM_014141.6(CNTNAP2):c.*2260C>A	rs186600344
NM_014141.6(CNTNAP2):c.*818dup	rs145690138
NM_014141.6(CNTNAP2):c.2356G>T (p.Val786Leu)	rs138517537

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