Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.146778124C>GCA578592079CNTNAP2c.208+3743C>G (p.=)
gnomAD
7g.146778126A>GCA578592080CNTNAP2c.208+3745A>G (p.=)
gnomAD
7g.146778127A>TCA834841261CNTNAP2c.208+3746A>T (p.=)
7g.146778131T>CCA834841262CNTNAP2c.208+3750T>C (p.=)
7g.146778144A>GCA168644836CNTNAP2c.208+3763A>G (p.=)
dbSNP gnomAD
7g.146778146G>ACA168644837CNTNAP2c.208+3765G>A (p.=)
dbSNP
7g.146778148A>GCA578592082CNTNAP2c.208+3767A>G (p.=)
gnomAD
7g.146778157G>ACA834841274CNTNAP2c.208+3776G>A (p.=)
7g.146778157G>TCA578592084CNTNAP2c.208+3776G>T (p.=)
gnomAD
7g.146778163C>ACA168644838CNTNAP2c.208+3782C>A (p.=)
dbSNP
7g.146778164A>GCA834841276CNTNAP2c.208+3783A>G (p.=)
7g.146778167A>GCA834841292CNTNAP2c.208+3786A>G (p.=)
7g.146778169G>ACA168644839CNTNAP2c.208+3788G>A (p.=)
dbSNP
7g.146778170T>CCA578592085CNTNAP2c.208+3789T>C (p.=)
gnomAD
7g.146778172G>ACA168644840CNTNAP2c.208+3791G>A (p.=)
dbSNP
7g.146778182G>ACA168644841CNTNAP2c.208+3801G>A (p.=)
dbSNP gnomAD
7g.146778185T>ACA578592088CNTNAP2c.208+3804T>A (p.=)
gnomAD
7g.146778201T>GCA652236803CNTNAP2c.208+3820T>G (p.=)
COSMIC
7g.146778206A>TCA578592089CNTNAP2c.208+3825A>T (p.=)
gnomAD
7g.146778208A>GCA168644842CNTNAP2c.208+3827A>G (p.=)
dbSNP
7g.146778214T>CCA168644843CNTNAP2c.208+3833T>C (p.=)
dbSNP
7g.146778222G>ACA168644844CNTNAP2c.208+3841G>A (p.=)
dbSNP gnomAD

Number of alleles fetched