List of variants in gene CNTNAP2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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_014141.6(CNTNAP2):c.2123T>C (p.Val708Ala)	rs148453565	0.00151
NM_014141.6(CNTNAP2):c.73G>A (p.Ala25Thr)	rs200866893	0.00101
NM_014141.6(CNTNAP2):c.136G>A (p.Val46Met)	rs137924687	0.00059
NM_014141.6(CNTNAP2):c.479G>A (p.Arg160His)	rs138738227	0.00048
NM_014141.6(CNTNAP2):c.3758T>C (p.Ile1253Thr)	rs767821521	0.00033
NM_014141.6(CNTNAP2):c.1145G>A (p.Ser382Asn)	rs371839994	0.00030
NM_014141.6(CNTNAP2):c.1786G>A (p.Glu596Lys)	rs141064983	0.00019
NM_014141.6(CNTNAP2):c.2096C>A (p.Pro699Gln)	rs764412489	0.00009
NM_014141.6(CNTNAP2):c.3155G>A (p.Arg1052His)	rs374739970	0.00009
NM_014141.6(CNTNAP2):c.653C>T (p.Thr218Met)	rs771028883	0.00007
NM_014141.6(CNTNAP2):c.1033G>A (p.Val345Ile)	rs145832489	0.00006
NM_014141.6(CNTNAP2):c.3112G>A (p.Asp1038Asn)	rs144003410	0.00006
NM_014141.6(CNTNAP2):c.3179C>T (p.Ala1060Val)	rs369254596	0.00006
NM_014141.6(CNTNAP2):c.3355C>T (p.Arg1119Cys)	rs367664952	0.00006
NM_014141.6(CNTNAP2):c.436G>A (p.Val146Ile)	rs781338949	0.00006
NM_014141.6(CNTNAP2):c.2239G>A (p.Ala747Thr)	rs150530671	0.00005
NM_014141.6(CNTNAP2):c.3271C>G (p.Leu1091Val)	rs756994633	0.00005
NM_014141.6(CNTNAP2):c.341G>A (p.Arg114Gln)	rs189731792	0.00005
NM_014141.6(CNTNAP2):c.1337A>G (p.Asp446Gly)	rs753860243	0.00003
NM_014141.6(CNTNAP2):c.416A>G (p.Asn139Ser)	rs370517200	0.00003
NM_014141.6(CNTNAP2):c.485T>G (p.Val162Gly)	rs587780320	0.00003
NM_014141.6(CNTNAP2):c.676C>A (p.Leu226Met)	rs372345438	0.00003
NM_014141.6(CNTNAP2):c.3106G>A (p.Ala1036Thr)	rs545175315	0.00001
NM_014141.6(CNTNAP2):c.3289C>T (p.Pro1097Ser)	rs200823464	0.00001
NM_014141.6(CNTNAP2):c.1709C>T (p.Ser570Leu)	rs377627481
NM_014141.6(CNTNAP2):c.1998C>A (p.Ser666Arg)	rs759797092
NM_014141.6(CNTNAP2):c.3595G>T (p.Ala1199Ser)	rs727503878
NM_014141.6(CNTNAP2):c.3862C>T (p.Arg1288Cys)	rs138661307
NM_014141.6(CNTNAP2):c.875T>A (p.Leu292Gln)	rs1801102530

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