ClinVar Miner

List of variants in gene SNCAIP reported as uncertain significance

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_005460.4(SNCAIP):c.-66C>T rs886059823 0.00028
NM_005460.4(SNCAIP):c.-46-6G>A rs375818767 0.00020
NM_005460.4(SNCAIP):c.1087G>A (p.Ala363Thr) rs145038921 0.00017
NM_005460.4(SNCAIP):c.786A>C (p.Thr262=) rs147831994 0.00007
NM_005460.4(SNCAIP):c.688A>G (p.Lys230Glu) rs374522874 0.00005
NM_005460.4(SNCAIP):c.204T>C (p.Asp68=) rs770583296 0.00004
NM_005460.4(SNCAIP):c.1002+7A>G rs574376579 0.00003
NM_005460.4(SNCAIP):c.198C>T (p.Ile66=) rs370204801 0.00003
NM_005460.4(SNCAIP):c.-47+3G>A rs886059824 0.00002
NM_005460.4(SNCAIP):c.-54C>A rs1418351789 0.00001
NM_005460.4(SNCAIP):c.1206C>T (p.Arg402=) rs1158148020 0.00001
NM_005460.4(SNCAIP):c.137G>A (p.Ser46Asn) rs1393526827 0.00001
NM_005460.4(SNCAIP):c.444C>T (p.Leu148=) rs762767013 0.00001
GRCh37/hg19 5q23.2(chr5:121581144-121713088)x1
GRCh37/hg19 5q23.2(chr5:121666151-121748939)x1
NM_005460.4(SNCAIP):c.-13G>T rs762576870
NM_005460.4(SNCAIP):c.-48G>A rs1580686722
NM_005460.4(SNCAIP):c.1002+2T>C rs1776845244
NM_005460.4(SNCAIP):c.104G>A (p.Cys35Tyr)
NM_005460.4(SNCAIP):c.1073C>T (p.Ala358Val)
NM_005460.4(SNCAIP):c.110C>T (p.Thr37Met)
NM_005460.4(SNCAIP):c.1118T>C (p.Met373Thr)
NM_005460.4(SNCAIP):c.113A>C (p.Gln38Pro)
NM_005460.4(SNCAIP):c.1175C>G (p.Ala392Gly)
NM_005460.4(SNCAIP):c.122A>G (p.Asp41Gly)
NM_005460.4(SNCAIP):c.1232T>C (p.Ile411Thr)
NM_005460.4(SNCAIP):c.1279G>T (p.Ala427Ser)
NM_005460.4(SNCAIP):c.150T>A (p.Asn50Lys)
NM_005460.4(SNCAIP):c.166C>T (p.Leu56Phe)
NM_005460.4(SNCAIP):c.190A>T (p.Thr64Ser)
NM_005460.4(SNCAIP):c.230A>G (p.Lys77Arg)
NM_005460.4(SNCAIP):c.261G>T (p.Glu87Asp)
NM_005460.4(SNCAIP):c.272A>G (p.Asn91Ser)
NM_005460.4(SNCAIP):c.286G>A (p.Asp96Asn)
NM_005460.4(SNCAIP):c.292A>G (p.Lys98Glu) rs1776706630
NM_005460.4(SNCAIP):c.298C>A (p.Gln100Lys)
NM_005460.4(SNCAIP):c.302A>G (p.Lys101Arg)
NM_005460.4(SNCAIP):c.326G>A (p.Gly109Asp)
NM_005460.4(SNCAIP):c.341G>A (p.Gly114Asp)
NM_005460.4(SNCAIP):c.382G>A (p.Gly128Ser)
NM_005460.4(SNCAIP):c.388C>T (p.Pro130Ser) rs1776726284
NM_005460.4(SNCAIP):c.409A>G (p.Ser137Gly)
NM_005460.4(SNCAIP):c.421G>C (p.Gly141Arg)
NM_005460.4(SNCAIP):c.429G>A (p.Leu143=) rs886059825
NM_005460.4(SNCAIP):c.446A>G (p.Asp149Gly)
NM_005460.4(SNCAIP):c.44G>A (p.Ser15Asn)
NM_005460.4(SNCAIP):c.503T>A (p.Phe168Tyr)
NM_005460.4(SNCAIP):c.530T>A (p.Ile177Asn)
NM_005460.4(SNCAIP):c.533T>G (p.Leu178Trp)
NM_005460.4(SNCAIP):c.598T>C (p.Ser200Pro)
NM_005460.4(SNCAIP):c.616C>T (p.Pro206Ser)
NM_005460.4(SNCAIP):c.709G>A (p.Glu237Lys) rs771056040
NM_005460.4(SNCAIP):c.730A>G (p.Lys244Glu)
NM_005460.4(SNCAIP):c.781A>C (p.Lys261Gln)
NM_005460.4(SNCAIP):c.785C>T (p.Thr262Ile)
NM_005460.4(SNCAIP):c.788T>G (p.Phe263Cys)
NM_005460.4(SNCAIP):c.7G>A (p.Ala3Thr)
NM_005460.4(SNCAIP):c.800A>G (p.His267Arg)
NM_005460.4(SNCAIP):c.853C>G (p.Leu285Val)
NM_005460.4(SNCAIP):c.908G>A (p.Arg303Gln)
NM_005460.4(SNCAIP):c.947T>C (p.Leu316Pro)
NM_005460.4(SNCAIP):c.974T>C (p.Ile325Thr)
NM_005460.4(SNCAIP):c.98G>A (p.Arg33Gln)

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