ClinVar Miner

List of variants in gene MTTP reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_001386140.1(MTTP):c.*1046C>G rs1061271 0.59509
NM_001386140.1(MTTP):c.453T>C (p.Gly151=) rs991811 0.47516
NM_001386140.1(MTTP):c.891C>G (p.His297Gln) rs2306985 0.47212
NM_001386140.1(MTTP):c.2513+94A>G rs881981 0.47162
NC_000004.12:g.99574660T>C rs1800804 0.26064
NM_001386140.1(MTTP):c.383T>C (p.Ile128Thr) rs3816873 0.26064
NM_001386140.1(MTTP):c.1990-29G>A rs2718684 0.19327
NM_001386140.1(MTTP):c.759-116A>G rs2306984 0.16623
NM_001386140.1(MTTP):c.1770-47A>T rs2298747 0.14139
NM_001386140.1(MTTP):c.522T>C (p.Cys174=) rs982424 0.12209
NM_001386140.1(MTTP):c.2514-89A>G rs2255119 0.11926
NM_001386140.1(MTTP):c.1990-157C>T rs41275715 0.10656
NM_001386140.1(MTTP):c.1989+192T>A rs745074 0.10655
NM_001386140.1(MTTP):c.2217+185A>T rs1491246 0.10651
NM_001386140.1(MTTP):c.1067+102A>T rs79194015 0.10650
NM_001386140.1(MTTP):c.2217+257T>G rs1491245 0.10646
NM_001386140.1(MTTP):c.1989+27T>C rs745075 0.10643
NM_001386140.1(MTTP):c.969T>C (p.Ala323=) rs17533489 0.10642
NM_001386140.1(MTTP):c.1068-85C>T rs17533517 0.10628
NM_001386140.1(MTTP):c.294G>C (p.Glu98Asp) rs2306986 0.08726
NM_001386140.1(MTTP):c.497A>G (p.Asn166Ser) rs3792683 0.08314
NM_001386140.1(MTTP):c.2343-51A>T rs1491244 0.08283
NM_001386140.1(MTTP):c.*183C>T rs74542928 0.08278
NM_001386140.1(MTTP):c.*862C>A rs6832927 0.08274
NM_001386140.1(MTTP):c.*506A>G rs6832119 0.08272
NM_001386140.1(MTTP):c.1237-172C>T rs34777713 0.07758
NM_001386140.1(MTTP):c.39C>G (p.Ser13=) rs7667001 0.07507
NM_001386140.1(MTTP):c.501+108G>A rs17029189 0.07369
NM_001386140.1(MTTP):c.1151A>C (p.Asp384Ala) rs17029215 0.07361
NM_001386140.1(MTTP):c.933C>A (p.Thr311=) rs17029213 0.07360
NM_001386140.1(MTTP):c.1769+9C>T rs34734558 0.07357
NM_001386140.1(MTTP):c.2218-32T>G rs41275719 0.07351
NM_001386140.1(MTTP):c.2513+190A>G rs574470118 0.07341
NM_001386140.1(MTTP):c.502-42C>T rs11734413 0.07291
NM_001386140.1(MTTP):c.394-32T>C rs3792681 0.06390
NM_001386140.1(MTTP):c.285G>C (p.Gln95His) rs61733139 0.04959
NM_001386140.1(MTTP):c.502-254C>T rs141186441 0.04349
NM_001386140.1(MTTP):c.394-250G>A rs145662623 0.04345
NM_001386140.1(MTTP):c.1237-85G>A rs114681504 0.04334
NM_001386140.1(MTTP):c.1769+14C>T rs41275713 0.03960
NM_001386140.1(MTTP):c.730C>G (p.Gln244Glu) rs17599091 0.03958
NM_001386140.1(MTTP):c.1237-225T>G rs116678836 0.03700
NM_001386140.1(MTTP):c.1981G>A (p.Gly661Ser) rs113337987 0.02355
NM_001386140.1(MTTP):c.660T>C (p.Tyr220=) rs113557405 0.02353
NM_001386140.1(MTTP):c.250-90T>C rs77010227 0.01633
NM_001386140.1(MTTP):c.136C>G (p.Arg46Gly) rs141736123 0.01357
NM_001386140.1(MTTP):c.2636A>G (p.Lys879Arg) rs114049933 0.01021
NM_001386140.1(MTTP):c.*515G>A rs116005476 0.00885
NM_001386140.1(MTTP):c.502G>A (p.Val168Ile) rs61750974 0.00763
NM_001386140.1(MTTP):c.2043G>A (p.Glu681=) rs145444300 0.00389
NM_001386140.1(MTTP):c.1731C>T (p.Ala577=) rs112506924 0.00290
NM_001386140.1(MTTP):c.1557+7T>A rs142706742 0.00266
NM_001386140.1(MTTP):c.2673C>T (p.Ser891=) rs115222767 0.00236
NM_001386140.1(MTTP):c.2513+13G>A rs148073215 0.00176
NM_001386140.1(MTTP):c.2025C>T (p.Ile675=) rs79023226 0.00123
NM_001386140.1(MTTP):c.1401A>G (p.Lys467=) rs148469697 0.00057
NM_001386140.1(MTTP):c.111G>A (p.Thr37=) rs147921439 0.00028
NM_001386140.1(MTTP):c.95G>A (p.Arg32Gln) rs199537553 0.00010
NC_000004.12:g.99574331G>T rs1800591
NM_001386140.1(MTTP):c.1068-108del rs5860584
NM_001386140.1(MTTP):c.1068-5del
NM_001386140.1(MTTP):c.1068-5dup rs752279560
NM_001386140.1(MTTP):c.1237-219_1237-134del rs1560621375
NM_001386140.1(MTTP):c.1557+191_1557+196del rs112760345
NM_001386140.1(MTTP):c.1557+264C>T rs76819189
NM_001386140.1(MTTP):c.1557+47_1557+48dup rs375598284
NM_001386140.1(MTTP):c.1557+48del rs375598284
NM_001386140.1(MTTP):c.1557+48dup rs375598284
NM_001386140.1(MTTP):c.1558-209C>T rs35779395
NM_001386140.1(MTTP):c.1715A>G (p.Asn572Ser) rs772602972
NM_001386140.1(MTTP):c.1770-68del rs5860586
NM_001386140.1(MTTP):c.2218-235T>C rs1032355
NM_001386140.1(MTTP):c.2218-8del
NM_001386140.1(MTTP):c.2218-8dup
NM_001386140.1(MTTP):c.2513+193del rs71600263
NM_001386140.1(MTTP):c.2513+235T>C rs41275721
NM_001386140.1(MTTP):c.394-6del
NM_001386140.1(MTTP):c.490A>G (p.Thr164Ala) rs563558722
NM_001386140.1(MTTP):c.61+136_61+137del rs3833621
NM_001386140.1(MTTP):c.62-240G>T rs28595160
NM_001386140.1(MTTP):c.758+81TG[7] rs34883891

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