ClinVar Miner

List of variants in gene NLRP7 reported as not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP
NM_001127255.1(NLRP7):c.-123C>T rs199475820
NM_001127255.1(NLRP7):c.-213G>T rs199475819
NM_001127255.1(NLRP7):c.-39-16C>T rs775886
NM_001127255.1(NLRP7):c.-39-300C>T rs10421217
NM_001127255.1(NLRP7):c.-39-393G>A rs10421098
NM_001127255.1(NLRP7):c.-39-427T>C rs104895519
NM_001127255.1(NLRP7):c.-39-4C>G rs199476227
NM_001127255.1(NLRP7):c.-39-792C>T rs143652352
NM_001127255.1(NLRP7):c.-39-90G>C rs376266895
NM_001127255.1(NLRP7):c.-40+21C>T rs703473
NM_001127255.1(NLRP7):c.-40+36C>T rs7248636
NM_001127255.1(NLRP7):c.1080C>A (p.Gly360=) rs199475825
NM_001127255.1(NLRP7):c.1137G>C (p.Lys379Asn) rs10418277
NM_001127255.1(NLRP7):c.1138G>C (p.Gly380Arg) rs104895557
NM_001127255.1(NLRP7):c.1148C>T (p.Pro383Leu) rs199475826
NM_001127255.1(NLRP7):c.1171A>G (p.Thr391Ala) rs199475827
NM_001127255.1(NLRP7):c.1193T>G (p.Leu398Arg) rs104895548
NM_001127255.1(NLRP7):c.1196G>A (p.Cys399Tyr) rs104895510
NM_001127255.1(NLRP7):c.1235T>C (p.Leu412Pro) rs199475828
NM_001127255.1(NLRP7):c.1294C>T (p.Arg432Ter) rs104895530
NM_001127255.1(NLRP7):c.1302C>T (p.Asp434=) rs104895545
NM_001127255.1(NLRP7):c.1456dup (p.Glu486fs) rs104895559
NM_001127255.1(NLRP7):c.1461G>A (p.Gly487=) rs199475829
NM_001127255.1(NLRP7):c.1708G>T (p.Glu570Ter) rs104895544
NM_001127255.1(NLRP7):c.1823C>T (p.Ser608Phe) rs199475830
NM_001127255.1(NLRP7):c.183del (p.Ser62fs) rs104895546
NM_001127255.1(NLRP7):c.1931+110T>C rs11879109
NM_001127255.1(NLRP7):c.1931+176G>T rs104895533
NM_001127255.1(NLRP7):c.1931+18A>T rs104895531
NM_001127255.1(NLRP7):c.1931+226C>G rs104895534
NM_001127255.1(NLRP7):c.1931+43C>T rs104895532
NM_001127255.1(NLRP7):c.1932-103G>C rs79420921
NM_001127255.1(NLRP7):c.1932-146C>T rs775879
NM_001127255.1(NLRP7):c.1932-178delT rs104895520
NM_001127255.1(NLRP7):c.1932-57T>C rs78894374
NM_001127255.1(NLRP7):c.1951C>T (p.Pro651Ser) rs104895549
NM_001127255.1(NLRP7):c.251G>A (p.Cys84Tyr) rs104895509
NM_001127255.1(NLRP7):c.295G>T (p.Glu99Ter) rs104895507
NM_001127255.1(NLRP7):c.337dup (p.Glu113fs) rs104895553
NM_001127255.1(NLRP7):c.346A>T (p.Lys116Ter) rs104895556
NM_001127255.1(NLRP7):c.352+1G>A rs104895504
NM_001127255.1(NLRP7):c.352+231G>A rs104895528
NM_001127255.1(NLRP7):c.353-111C>T rs62124617
NM_001127255.1(NLRP7):c.353-178A>G rs8106927
NM_001127255.1(NLRP7):c.353-216C>G rs8106278
NM_001127255.1(NLRP7):c.353-235C>T rs104895527
NM_001127255.1(NLRP7):c.446A>G (p.Asp149Gly) rs199475822
NM_001127255.1(NLRP7):c.516C>T (p.Tyr172=) rs199475823
NM_001127255.1(NLRP7):c.574A>C (p.Met192Leu) rs104895529
NM_001127255.1(NLRP7):c.701T>C (p.Leu234Ser) rs61732584
NM_001127255.1(NLRP7):c.719G>A (p.Ser240Asn) rs199475824
NM_001127255.1(NLRP7):c.915A>C (p.Ala305=) rs104895560
NM_001127255.1(NLRP7):c.939_952dup (p.Tyr318fs) rs104895547
NM_001127255.1(NLRP7):c.985A>C (p.Arg329=) rs104895511
NM_001127255.1(NLRP7):c.9G>A (p.Ser3=) rs199475821

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