ClinVar Miner

List of variants in gene BMPR1A reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 73
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HGVS dbSNP
NM_004329.2(BMPR1A):c.1017C>G (p.Ala339=) rs780130011
NM_004329.2(BMPR1A):c.102G>A (p.Gly34=) rs876659958
NM_004329.2(BMPR1A):c.1059A>G (p.Gln353=) rs1060503407
NM_004329.2(BMPR1A):c.1068C>T (p.Pro356=) rs759520915
NM_004329.2(BMPR1A):c.1086C>T (p.Asp362=) rs201415408
NM_004329.2(BMPR1A):c.1141C>T (p.Leu381=) rs864622566
NM_004329.2(BMPR1A):c.1146C>A (p.Gly382=) rs786203626
NM_004329.2(BMPR1A):c.1173A>T (p.Thr391=) rs766032673
NM_004329.2(BMPR1A):c.117C>G (p.Ser39=) rs757333646
NM_004329.2(BMPR1A):c.117C>T (p.Ser39=) rs757333646
NM_004329.2(BMPR1A):c.1191C>G (p.Pro397=) rs751078831
NM_004329.2(BMPR1A):c.1230C>T (p.Pro410=) rs200642188
NM_004329.2(BMPR1A):c.1243G>A (p.Glu415Lys) rs140592056
NM_004329.2(BMPR1A):c.1249C>T (p.Leu417=) rs1554891334
NM_004329.2(BMPR1A):c.1251G>A (p.Leu417=) rs1554891336
NM_004329.2(BMPR1A):c.1266C>T (p.Phe422=) rs786202823
NM_004329.2(BMPR1A):c.126A>G (p.Lys42=) rs773814289
NM_004329.2(BMPR1A):c.1287C>T (p.Asp429=) rs777021606
NM_004329.2(BMPR1A):c.12A>G (p.Leu4=) rs772729006
NM_004329.2(BMPR1A):c.132A>C (p.Ser44=) rs1554888111
NM_004329.2(BMPR1A):c.1347C>T (p.Ile449=) rs1057520966
NM_004329.2(BMPR1A):c.1348G>A (p.Val450Met) rs55932635
NM_004329.2(BMPR1A):c.1359C>T (p.Tyr453=) rs876660878
NM_004329.2(BMPR1A):c.1362A>G (p.Gln454=) rs764090248
NM_004329.2(BMPR1A):c.1368A>G (p.Pro456=) rs864622447
NM_004329.2(BMPR1A):c.1386G>A (p.Pro462=) rs751815388
NM_004329.2(BMPR1A):c.1395G>A (p.Pro465=) rs55845713
NM_004329.2(BMPR1A):c.1395G>C (p.Pro465=) rs55845713
NM_004329.2(BMPR1A):c.1398A>C (p.Ser466=) rs56410735
NM_004329.2(BMPR1A):c.1401C>T (p.Tyr467=) rs149787558
NM_004329.2(BMPR1A):c.1419T>G (p.Val473=) rs145756629
NM_004329.2(BMPR1A):c.1449G>T (p.Val483=) rs759740989
NM_004329.2(BMPR1A):c.1479A>G (p.Leu493=) rs1554891640
NM_004329.2(BMPR1A):c.148T>C (p.Leu50=) rs964544915
NM_004329.2(BMPR1A):c.1536C>T (p.Leu512=) rs758796892
NM_004329.2(BMPR1A):c.1560G>A (p.Thr520=) rs142775086
NM_004329.2(BMPR1A):c.1569G>A (p.Lys523=) rs876659703
NM_004329.2(BMPR1A):c.183C>T (p.Cys61=) rs140610221
NM_004329.2(BMPR1A):c.195G>A (p.Gly65=) rs765437517
NM_004329.2(BMPR1A):c.195G>C (p.Gly65=) rs765437517
NM_004329.2(BMPR1A):c.213T>C (p.Ala71=) rs1554888138
NM_004329.2(BMPR1A):c.285A>G (p.Thr95=) rs1473234057
NM_004329.2(BMPR1A):c.294A>G (p.Ser98=) rs764466269
NM_004329.2(BMPR1A):c.30A>G (p.Leu10=) rs754752449
NM_004329.2(BMPR1A):c.33G>A (p.Leu11=) rs535411352
NM_004329.2(BMPR1A):c.415C>T (p.Pro139Ser) rs772163112
NM_004329.2(BMPR1A):c.499A>G (p.Met167Val) rs200951235
NM_004329.2(BMPR1A):c.510C>T (p.Phe170=) rs747266339
NM_004329.2(BMPR1A):c.558A>G (p.Arg186=) rs752388441
NM_004329.2(BMPR1A):c.560G>A (p.Arg187His) rs189059377
NM_004329.2(BMPR1A):c.59G>A (p.Arg20His) rs759014147
NM_004329.2(BMPR1A):c.600T>C (p.Ile200=) rs876659999
NM_004329.2(BMPR1A):c.618A>G (p.Leu206=) rs55992440
NM_004329.2(BMPR1A):c.663A>C (p.Gly221=) rs1462920023
NM_004329.2(BMPR1A):c.676-5T>C rs200537780
NM_004329.2(BMPR1A):c.682C>A (p.Arg228=) rs587782682
NM_004329.2(BMPR1A):c.744A>G (p.Val248=) rs1060504910
NM_004329.2(BMPR1A):c.760C>T (p.Arg254Cys) rs587782578
NM_004329.2(BMPR1A):c.765C>T (p.Gly255=) rs786201114
NM_004329.2(BMPR1A):c.777G>A (p.Ala259=) rs56108371
NM_004329.2(BMPR1A):c.789C>T (p.Phe263=) rs771932684
NM_004329.2(BMPR1A):c.828A>G (p.Glu276=) rs1554890804
NM_004329.2(BMPR1A):c.831C>A (p.Ile277=) rs876659520
NM_004329.2(BMPR1A):c.879G>A (p.Ala293=) rs770203548
NM_004329.2(BMPR1A):c.879G>C (p.Ala293=) rs770203548
NM_004329.2(BMPR1A):c.909T>C (p.Thr303=) rs1554891026
NM_004329.2(BMPR1A):c.927T>C (p.Thr309=) rs779691540
NM_004329.2(BMPR1A):c.93T>C (p.His31=) rs1461705514
NM_004329.2(BMPR1A):c.951C>T (p.Leu317=) rs908671564
NM_004329.2(BMPR1A):c.961C>T (p.Leu321=) rs377412651
NM_004329.2(BMPR1A):c.98C>G (p.Thr33Ser) rs142454490
NM_004329.2(BMPR1A):c.990C>T (p.Ala330=) rs199808362
NM_004329.2(BMPR1A):c.993G>A (p.Leu331=) rs786202827

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