ClinVar Miner

List of variants in gene NLGN4X reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_181332.3(NLGN4X):c.392A>G (p.Asn131Ser) rs145307351 0.00057
NM_181332.3(NLGN4X):c.1133A>G (p.Lys378Arg) rs144093574 0.00028
NM_181332.3(NLGN4X):c.1305G>A (p.Thr435=) rs149512448 0.00023
NM_181332.3(NLGN4X):c.2360C>T (p.Thr787Met) rs4995611 0.00016
NM_181332.3(NLGN4X):c.1544A>G (p.Asn515Ser) rs138545443 0.00011
NM_181332.3(NLGN4X):c.1887C>T (p.Pro629=) rs778014568 0.00008
NM_181332.3(NLGN4X):c.936G>A (p.Thr312=) rs201720833 0.00008
NM_181332.3(NLGN4X):c.2178C>T (p.Asn726=) rs187221748 0.00006
NM_181332.3(NLGN4X):c.48G>A (p.Pro16=) rs398124365 0.00006
NM_181332.3(NLGN4X):c.1877G>A (p.Arg626Gln) rs1291813149 0.00003
NM_181332.3(NLGN4X):c.1197G>C (p.Val399=) rs1456373848 0.00001
NM_181332.3(NLGN4X):c.1356C>T (p.Pro452=) rs111519296 0.00001
NM_181332.3(NLGN4X):c.2297G>A (p.Arg766Gln) rs1445553567 0.00001
NM_181332.3(NLGN4X):c.71A>G (p.Asn24Ser) rs775784070 0.00001
NM_181332.3(NLGN4X):c.1053C>T (p.Asp351=)
NM_181332.3(NLGN4X):c.10C>T (p.Pro4Ser)
NM_181332.3(NLGN4X):c.1110C>T (p.Gly370=)
NM_181332.3(NLGN4X):c.1143C>T (p.Asp381=)
NM_181332.3(NLGN4X):c.1181A>G (p.Asp394Gly)
NM_181332.3(NLGN4X):c.1216C>A (p.Leu406Ile) rs886044072
NM_181332.3(NLGN4X):c.1418A>G (p.Tyr473Cys)
NM_181332.3(NLGN4X):c.1477G>A (p.Val493Ile) rs2031978800
NM_181332.3(NLGN4X):c.1491C>T (p.Phe497=)
NM_181332.3(NLGN4X):c.1548C>T (p.Asp516=)
NM_181332.3(NLGN4X):c.1829C>T (p.Thr610Ile) rs2146686298
NM_181332.3(NLGN4X):c.187C>A (p.Pro63Thr) rs150566193
NM_181332.3(NLGN4X):c.2019C>T (p.Thr673=)
NM_181332.3(NLGN4X):c.2055C>G (p.Leu685=)
NM_181332.3(NLGN4X):c.2194C>T (p.Leu732=)
NM_181332.3(NLGN4X):c.2325G>A (p.Thr775=)
NM_181332.3(NLGN4X):c.411C>T (p.Thr137=)
NM_181332.3(NLGN4X):c.473-3273G>A
NM_181332.3(NLGN4X):c.473-5dup rs766542143
NM_181332.3(NLGN4X):c.542C>T (p.Thr181Ile)
NM_181332.3(NLGN4X):c.819C>T (p.Phe273=)
NM_181332.3(NLGN4X):c.846C>T (p.Thr282=)
NM_181332.3(NLGN4X):c.949T>C (p.Cys317Arg) rs1064797357

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