ClinVar Miner

List of variants in gene FSIP2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_173651.4(FSIP2):c.19772C>T (p.Thr6591Ile) rs201876794 0.00395
NM_173651.4(FSIP2):c.9739A>G (p.Arg3247Gly) rs142306380 0.00246
NM_173651.4(FSIP2):c.6226C>A (p.Leu2076Met) rs74508015 0.00236
NM_173651.4(FSIP2):c.9536A>G (p.Asn3179Ser) rs115715789 0.00236
NM_173651.4(FSIP2):c.16542G>C (p.Val5514=) rs184298485 0.00172
NM_173651.4(FSIP2):c.19356A>G (p.Lys6452=) rs200925453 0.00146
NM_173651.4(FSIP2):c.4597T>A (p.Ser1533Thr) rs200352552 0.00027
NM_173651.4(FSIP2):c.19032T>C (p.Asp6344=) rs200393690 0.00024
NM_173651.4(FSIP2):c.1770G>A (p.Thr590=) rs139442712 0.00016
NM_173651.4(FSIP2):c.10470C>T (p.Tyr3490=)
NM_173651.4(FSIP2):c.11963C>T (p.Ser3988Phe)
NM_173651.4(FSIP2):c.12168G>A (p.Gln4056=)
NM_173651.4(FSIP2):c.1217A>T (p.Asn406Ile)
NM_173651.4(FSIP2):c.12713G>A (p.Arg4238Gln)
NM_173651.4(FSIP2):c.13827A>G (p.Arg4609=)
NM_173651.4(FSIP2):c.14043G>A (p.Glu4681=)
NM_173651.4(FSIP2):c.14268T>C (p.His4756=)
NM_173651.4(FSIP2):c.14900A>T (p.Asn4967Ile)
NM_173651.4(FSIP2):c.15568T>C (p.Leu5190=)
NM_173651.4(FSIP2):c.16488T>C (p.Asn5496=)
NM_173651.4(FSIP2):c.16503C>T (p.Ser5501=) rs137864187
NM_173651.4(FSIP2):c.1703A>T (p.Tyr568Phe)
NM_173651.4(FSIP2):c.17198A>T (p.Lys5733Ile)
NM_173651.4(FSIP2):c.171G>T (p.Leu57=)
NM_173651.4(FSIP2):c.17823T>C (p.Asn5941=)
NM_173651.4(FSIP2):c.18447C>T (p.Ile6149=)
NM_173651.4(FSIP2):c.19209T>C (p.Ser6403=)
NM_173651.4(FSIP2):c.19452C>T (p.Asp6484=)
NM_173651.4(FSIP2):c.19692T>C (p.His6564=)
NM_173651.4(FSIP2):c.2223A>G (p.Glu741=)
NM_173651.4(FSIP2):c.309A>T (p.Pro103=)
NM_173651.4(FSIP2):c.4316C>G (p.Thr1439Arg)
NM_173651.4(FSIP2):c.4487GTG[1] (p.Gly1497del) rs748959283
NM_173651.4(FSIP2):c.7029A>G (p.Leu2343=)
NM_173651.4(FSIP2):c.7713T>C (p.Ser2571=)
NM_173651.4(FSIP2):c.9399T>C (p.Asn3133=)

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