ClinVar Miner

List of variants in gene CRPPA reported as uncertain significance for not provided

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Total variants: 88
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HGVS dbSNP
GRCh37/hg19 7p21.2(chr7:16346542-16403855)x1
NM_001101426.4(CRPPA):c.1026+1G>T rs1554300301
NM_001101426.4(CRPPA):c.1027-7C>T rs1453881839
NM_001101426.4(CRPPA):c.1058A>G (p.Lys353Arg) rs777155055
NM_001101426.4(CRPPA):c.1120-4G>A rs886042445
NM_001101426.4(CRPPA):c.1147C>A (p.Pro383Thr)
NM_001101426.4(CRPPA):c.1151C>T (p.Pro384Leu) rs752622525
NM_001101426.4(CRPPA):c.1161A>T (p.Lys387Asn) rs368477537
NM_001101426.4(CRPPA):c.117G>C (p.Glu39Asp)
NM_001101426.4(CRPPA):c.1192G>A (p.Ala398Thr)
NM_001101426.4(CRPPA):c.1218T>G (p.Ile406Met) rs202011820
NM_001101426.4(CRPPA):c.1234C>G (p.Leu412Val) rs747967711
NM_001101426.4(CRPPA):c.123G>C (p.Gly41=) rs761842188
NM_001101426.4(CRPPA):c.1246C>T (p.Pro416Ser) rs373134516
NM_001101426.4(CRPPA):c.1251+4G>A rs753402341
NM_001101426.4(CRPPA):c.1253A>G (p.Asp418Gly) rs1174210413
NM_001101426.4(CRPPA):c.1264C>T (p.Leu422=)
NM_001101426.4(CRPPA):c.1301C>T (p.Ala434Val) rs886044370
NM_001101426.4(CRPPA):c.1307T>C (p.Leu436Ser) rs886044546
NM_001101426.4(CRPPA):c.136G>C (p.Ala46Pro) rs886043286
NM_001101426.4(CRPPA):c.139G>A (p.Val47Met) rs886043960
NM_001101426.4(CRPPA):c.160G>A (p.Gly54Arg)
NM_001101426.4(CRPPA):c.161G>T (p.Gly54Val) rs587777797
NM_001101426.4(CRPPA):c.17C>T (p.Pro6Leu) rs886043968
NM_001101426.4(CRPPA):c.191C>T (p.Thr64Ile) rs886042368
NM_001101426.4(CRPPA):c.193C>T (p.Pro65Ser) rs886042489
NM_001101426.4(CRPPA):c.200A>C (p.Gln67Pro) rs886043637
NM_001101426.4(CRPPA):c.209C>G (p.Pro70Arg) rs886042746
NM_001101426.4(CRPPA):c.20G>A (p.Gly7Asp) rs1562697191
NM_001101426.4(CRPPA):c.221G>C (p.Arg74Thr) rs1292380177
NM_001101426.4(CRPPA):c.239C>A (p.Thr80Asn) rs886044479
NM_001101426.4(CRPPA):c.243A>G (p.Leu81=)
NM_001101426.4(CRPPA):c.248C>T (p.Ala83Val) rs886044513
NM_001101426.4(CRPPA):c.24C>T (p.Ser8=) rs886043980
NM_001101426.4(CRPPA):c.255G>A (p.Glu85=) rs886042759
NM_001101426.4(CRPPA):c.258-3T>G rs899936625
NM_001101426.4(CRPPA):c.261A>G (p.Val87=) rs886044356
NM_001101426.4(CRPPA):c.277A>G (p.Ile93Val) rs762370550
NM_001101426.4(CRPPA):c.277_279del (p.Ile93del) rs397515398
NM_001101426.4(CRPPA):c.28A>T (p.Arg10Trp) rs886044165
NM_001101426.4(CRPPA):c.307G>A (p.Glu103Lys) rs775902619
NM_001101426.4(CRPPA):c.320G>T (p.Ser107Ile) rs199691459
NM_001101426.4(CRPPA):c.322_324ATT[1] (p.Ile109del) rs1554364074
NM_001101426.4(CRPPA):c.347G>A (p.Arg116His)
NM_001101426.4(CRPPA):c.382A>C (p.Arg128=) rs765435429
NM_001101426.4(CRPPA):c.382A>G (p.Arg128Gly)
NM_001101426.4(CRPPA):c.402A>G (p.Leu134=) rs368815582
NM_001101426.4(CRPPA):c.425T>A (p.Ile142Asn) rs1554363950
NM_001101426.4(CRPPA):c.44G>T (p.Gly15Val) rs573488291
NM_001101426.4(CRPPA):c.52C>T (p.Leu18=) rs886043287
NM_001101426.4(CRPPA):c.531C>T (p.His177=) rs376195897
NM_001101426.4(CRPPA):c.532G>A (p.Gly178Arg) rs202108204
NM_001101426.4(CRPPA):c.551G>A (p.Arg184Gln) rs773739293
NM_001101426.4(CRPPA):c.560T>C (p.Val187Ala) rs1554347337
NM_001101426.4(CRPPA):c.561A>G (p.Val187=) rs376375569
NM_001101426.4(CRPPA):c.602A>T (p.Tyr201Phe) rs1198960792
NM_001101426.4(CRPPA):c.636A>C (p.Glu212Asp) rs1008210645
NM_001101426.4(CRPPA):c.640C>T (p.Pro214Ser) rs886043226
NM_001101426.4(CRPPA):c.645A>G (p.Gln215=) rs532057629
NM_001101426.4(CRPPA):c.668A>G (p.Tyr223Cys) rs1364759577
NM_001101426.4(CRPPA):c.677A>G (p.Tyr226Cys) rs1289931198
NM_001101426.4(CRPPA):c.713C>T (p.Thr238Ile) rs397515409
NM_001101426.4(CRPPA):c.715G>A (p.Glu239Lys)
NM_001101426.4(CRPPA):c.779A>G (p.Asp260Gly) rs1554320085
NM_001101426.4(CRPPA):c.77A>C (p.His26Pro) rs886044190
NM_001101426.4(CRPPA):c.789+9G>A rs375132134
NM_001101426.4(CRPPA):c.7G>C (p.Ala3Pro)
NM_001101426.4(CRPPA):c.7G>T (p.Ala3Ser) rs794726893
NM_001101426.4(CRPPA):c.808C>T (p.Leu270Phe) rs200334999
NM_001101426.4(CRPPA):c.822A>T (p.Glu274Asp) rs886042675
NM_001101426.4(CRPPA):c.825G>A (p.Ser275=) rs766874330
NM_001101426.4(CRPPA):c.828T>C (p.Ile276=) rs201334104
NM_001101426.4(CRPPA):c.836-9T>A
NM_001101426.4(CRPPA):c.839G>T (p.Arg280Ile) rs761189549
NM_001101426.4(CRPPA):c.840A>G (p.Arg280=) rs148054819
NM_001101426.4(CRPPA):c.859G>A (p.Val287Ile) rs1562603622
NM_001101426.4(CRPPA):c.872C>A (p.Thr291Lys)
NM_001101426.4(CRPPA):c.881A>G (p.Asp294Gly) rs547473863
NM_001101426.4(CRPPA):c.890A>C (p.His297Pro) rs1562603563
NM_001101426.4(CRPPA):c.914T>G (p.Val305Gly) rs370397489
NM_001101426.4(CRPPA):c.915G>A (p.Val305=) rs1466053365
NM_001101426.4(CRPPA):c.934-5A>G rs886043337
NM_001101426.4(CRPPA):c.948A>G (p.Thr316=) rs780620823
NM_001101426.4(CRPPA):c.972C>A (p.Gly324=) rs370052768
NM_001101426.4(CRPPA):c.978T>A (p.His326Gln) rs901037542
NM_001101426.4(CRPPA):c.979C>G (p.Leu327Val) rs587780361
NM_001101426.4(CRPPA):c.991A>G (p.Ile331Val) rs886044693
NM_001101426.4(CRPPA):c.999T>C (p.Asp333=) rs376909665

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