ClinVar Miner

List of variants in gene CIC reported as not provided

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Total variants: 31
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HGVS dbSNP
NM_015125.4(CIC):c.1375G>A (p.Gly459Ser) rs141764284
NM_015125.4(CIC):c.1430G>C (p.Gly477Ala) rs201078050
NM_015125.4(CIC):c.1573G>A (p.Gly525Ser) rs150975726
NM_015125.4(CIC):c.1694_1695delinsAA (p.Gly565Glu) rs587778195
NM_015125.4(CIC):c.1909_1911del (p.Lys637del) rs587778196
NM_015125.4(CIC):c.1927G>A (p.Gly643Ser) rs587778199
NM_015125.4(CIC):c.1979C>T (p.Pro660Leu) rs139337301
NM_015125.4(CIC):c.2105A>G (p.Asn702Ser) rs202135824
NM_015125.4(CIC):c.2146C>T (p.Arg716Trp) rs537583557
NM_015125.4(CIC):c.2201C>T (p.Ser734Leu) rs587778197
NM_015125.4(CIC):c.2318C>T (p.Pro773Leu) rs587778198
NM_015125.4(CIC):c.2389G>A (p.Gly797Ser) rs587778200
NM_015125.4(CIC):c.2677C>T (p.Pro893Ser) rs142397024
NM_015125.4(CIC):c.2687C>T (p.Pro896Leu) rs549004026
NM_015125.4(CIC):c.2918C>A (p.Thr973Lys) rs543847978
NM_015125.4(CIC):c.2956C>G (p.Leu986Val) rs143825601
NM_015125.4(CIC):c.3202G>A (p.Gly1068Ser) rs370377701
NM_015125.4(CIC):c.3310T>A (p.Ser1104Thr) rs185048610
NM_015125.4(CIC):c.3485A>C (p.Tyr1162Ser) rs556245581
NM_015125.4(CIC):c.3553G>A (p.Ala1185Thr) rs587778202
NM_015125.4(CIC):c.3602G>A (p.Gly1201Asp) rs587778203
NM_015125.4(CIC):c.3658G>C (p.Glu1220Gln) rs587778204
NM_015125.4(CIC):c.3730C>T (p.Arg1244Trp) rs587778201
NM_015125.4(CIC):c.3829C>T (p.Arg1277Cys) rs587778206
NM_015125.4(CIC):c.3925A>G (p.Ser1309Gly) rs587778205
NM_015125.4(CIC):c.3956C>T (p.Pro1319Leu) rs587778207
NM_015125.4(CIC):c.4487G>A (p.Arg1496His) rs200799936
NM_015125.4(CIC):c.4616C>T (p.Pro1539Leu) rs587778208
NM_015125.4(CIC):c.463A>G (p.Ile155Val) rs199958449
NM_015125.4(CIC):c.551C>T (p.Ser184Phe) rs587778209
NM_015125.4(CIC):c.884C>T (p.Thr295Met) rs141544536

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