Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.146778222G>ACA168644844CNTNAP2c.208+3841G>A (p.=)
dbSNP gnomAD
7g.146778225C>TCA834841320CNTNAP2c.208+3844C>T (p.=)
7g.146778227T>CCA168644845CNTNAP2c.208+3846T>C (p.=)
dbSNP
7g.146778231G>CCA834841321CNTNAP2c.208+3850G>C (p.=)
7g.146778236G>ACA168644846CNTNAP2c.208+3855G>A (p.=)
dbSNP gnomAD
7g.146778238A>GCA168644847CNTNAP2c.208+3857A>G (p.=)
dbSNP
7g.146778244A>GCA168644848CNTNAP2c.208+3863A>G (p.=)
dbSNP gnomAD
7g.146778247A>CCA168644849CNTNAP2c.208+3866A>C (p.=)
dbSNP
7g.146778247A>GCA834841327CNTNAP2c.208+3866A>G (p.=)
7g.146778266T>CCA168644850CNTNAP2c.208+3885T>C (p.=)
dbSNP
7g.146778284A>CCA834841335CNTNAP2c.208+3903A>C (p.=)
7g.146778284A>TCA168644851CNTNAP2c.208+3903A>T (p.=)
dbSNP gnomAD
7g.146778285A>GCA578592090CNTNAP2c.208+3904A>G (p.=)
gnomAD
7g.146778286T>ACA168644852CNTNAP2c.208+3905T>A (p.=)
dbSNP
7g.146778286T>CCA168644853CNTNAP2c.208+3905T>C (p.=)
dbSNP
7g.146778289C>ACA834841340CNTNAP2c.208+3908C>A (p.=)
7g.146778294T>ACA168644854CNTNAP2c.208+3913T>A (p.=)
dbSNP gnomAD
7g.146778300A>GCA834841347CNTNAP2c.208+3919A>G (p.=)
7g.146778303T>CCA168644855CNTNAP2c.208+3922T>C (p.=)
dbSNP
7g.146778306A>GCA834841350CNTNAP2c.208+3925A>G (p.=)
7g.146778310A>TCA168644856CNTNAP2c.208+3929A>T (p.=)
dbSNP
7g.146778314G>TCA168644857CNTNAP2c.208+3933G>T (p.=)
dbSNP
7g.146778319dupCA834841353CNTNAP2c.208+3938dup (p.=)
7g.146778321G>CCA168644858CNTNAP2c.208+3940G>C (p.=)
dbSNP gnomAD

Number of alleles fetched