ClinVar Miner

List of variants in gene CNTNAP2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
Download table as spreadsheet
HGVS dbSNP
NM_014141.6(CNTNAP2):c.*1017T>G rs77001133
NM_014141.6(CNTNAP2):c.*1276_*1280dup rs369615005
NM_014141.6(CNTNAP2):c.*1433A>G rs78484397
NM_014141.6(CNTNAP2):c.*1482A>T rs186254614
NM_014141.6(CNTNAP2):c.*2151A>G rs28369221
NM_014141.6(CNTNAP2):c.*2260C>A
NM_014141.6(CNTNAP2):c.*2665C>T rs7791181
NM_014141.6(CNTNAP2):c.*2875dup rs138367128
NM_014141.6(CNTNAP2):c.*3392C>T rs115420302
NM_014141.6(CNTNAP2):c.*3433G>A rs142623983
NM_014141.6(CNTNAP2):c.*3531G>A rs79360609
NM_014141.6(CNTNAP2):c.*3540G>A rs114585910
NM_014141.6(CNTNAP2):c.*3796C>T rs183556756
NM_014141.6(CNTNAP2):c.*3921G>A rs141005348
NM_014141.6(CNTNAP2):c.*4071G>A rs147886818
NM_014141.6(CNTNAP2):c.*48G>A rs78018010
NM_014141.6(CNTNAP2):c.*818dup rs145690138
NM_014141.6(CNTNAP2):c.1220A>G (p.Asn407Ser) rs143877693
NM_014141.6(CNTNAP2):c.1710G>A (p.Ser570=) rs2286128
NM_014141.6(CNTNAP2):c.1854C>T (p.Gly618=) rs61732849
NM_014141.6(CNTNAP2):c.2099-15T>C rs75858942
NM_014141.6(CNTNAP2):c.2190C>T (p.Cys730=) rs74354654
NM_014141.6(CNTNAP2):c.2256-6A>T rs10240482
NM_014141.6(CNTNAP2):c.2356G>T (p.Val786Leu) rs138517537
NM_014141.6(CNTNAP2):c.3105C>T (p.Asn1035=) rs112483670
NM_014141.6(CNTNAP2):c.318C>T (p.Ser106=) rs61732853
NM_014141.6(CNTNAP2):c.341G>A (p.Arg114Gln) rs189731792
NM_014141.6(CNTNAP2):c.3476-15C>A rs77706740
NM_014141.6(CNTNAP2):c.3716-6C>G rs77025884
NM_014141.6(CNTNAP2):c.3797-6C>T rs79777576
NM_014141.6(CNTNAP2):c.515T>C (p.Ile172Thr) rs201326295
NM_014141.6(CNTNAP2):c.681C>T (p.His227=) rs142984073

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.