ClinVar Miner

List of variants studied for diaphragm disorder

Included ClinVar conditions (16):
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_181458.4(PAX3):c.944C>A (p.Thr315Lys) rs2234675 0.02573
NM_001927.4(DES):c.638C>T (p.Ala213Val) rs41272699 0.01015
NM_000245.4(MET):c.2975C>T (p.Thr992Ile) rs56391007 0.00911
NM_012082.4(ZFPM2):c.40+12C>G rs149902904 0.00711
NM_025074.7(FRAS1):c.9806G>A (p.Arg3269Gln) rs61729366 0.00592
NM_207361.6(FREM2):c.4031G>A (p.Arg1344His) rs143044921 0.00430
NM_012082.4(ZFPM2):c.89A>G (p.Glu30Gly) rs121908601 0.00293
NM_016239.4(MYO15A):c.1454T>C (p.Val485Ala) rs200532919 0.00079
NM_012082.4(ZFPM2):c.2963A>C (p.Lys988Thr) rs139881948 0.00073
NM_012082.4(ZFPM2):c.2107A>C (p.Met703Leu) rs121908603 0.00019
NM_001004356.3(FGFRL1):c.1328G>C (p.Gly443Ala) rs759581394 0.00011
NM_025074.7(FRAS1):c.2389G>A (p.Glu797Lys) rs372359356 0.00004
NM_000168.6(GLI3):c.2726C>G (p.Ala909Gly) rs780263938 0.00001
NM_001004356.3(FGFRL1):c.886A>G (p.Ile296Val) rs753437773 0.00001
NM_001244008.2(KIF1A):c.3052C>T (p.His1018Tyr) rs1356639316 0.00001
NM_006005.3(WFS1):c.1999C>T (p.Gln667Ter) rs771409809 0.00001
NM_012082.4(ZFPM2):c.334C>T (p.Arg112Ter) rs121908602 0.00001
NM_019055.6(ROBO4):c.569G>C (p.Gly190Ala) rs756636036 0.00001
NM_025074.7(FRAS1):c.6323A>T (p.Asp2108Val) rs921444831 0.00001
46;X;t(X;10)(p11.2;q24.3)
46;XX;t(7;13)(p13;q34)dn
46;XY;t(1;6)(p22;q15)dn
GRCh38/hg38 17q12(chr17:36719878-37889304)
NM_000138.5(FBN1):c.4970_4971insA (p.Cys1658fs) rs864309713
NM_001127392.3(MYRF):c.1209G>C (p.Gln403His) rs1027079885
NM_001127392.3(MYRF):c.1303G>A (p.Gly435Arg) rs1565295550
NM_001127392.3(MYRF):c.1904-1G>A rs2066445430
NM_001127392.3(MYRF):c.2036T>C (p.Val679Ala) rs2066476390
NM_001127392.3(MYRF):c.2084G>A (p.Arg695His) rs1382225004
NM_001127392.3(MYRF):c.239dup (p.Gly81fs) rs2066051319
NM_001242896.3(DEPDC5):c.2785G>A (p.Gly929Ser) rs1569084151
NM_001260.3(CDK8):c.185C>A (p.Ser62Ter) rs1565977796
NM_001379081.2(FREM1):c.1394G>C (p.Gly465Ala) rs41298151
NM_001822.7(CHN1):c.667G>A (p.Ala223Thr) rs1558939623
NM_002430.3(MN1):c.3839del (p.Cys1280fs) rs1601319594
NM_003888.4(ALDH1A2):c.1040G>A (p.Arg347His)
NM_003888.4(ALDH1A2):c.1147G>A (p.Ala383Thr)
NM_003888.4(ALDH1A2):c.1382C>A (p.Ser461Tyr)
NM_003888.4(ALDH1A2):c.544C>A (p.Gln182Lys)
NM_005032.7(PLS3):c.1054T>C (p.Phe352Leu) rs2147577404
NM_005032.7(PLS3):c.1090A>G (p.Lys364Glu)
NM_005032.7(PLS3):c.1497G>C (p.Trp499Cys)
NM_005032.7(PLS3):c.1774A>G (p.Met592Val)
NM_005032.7(PLS3):c.359C>T (p.Ser120Phe)
NM_005032.7(PLS3):c.617C>T (p.Ala206Val) rs2147551760
NM_005032.7(PLS3):c.808G>A (p.Glu270Lys)
NM_005257.6(GATA6):c.1072del (p.Val358fs) rs1555628863
NM_005257.6(GATA6):c.1366C>T (p.Arg456Cys) rs387906818
NM_005257.6(GATA6):c.712G>T (p.Gly238Ter) rs587777710
NM_006218.4(PIK3CA):c.1030G>A (p.Val344Met) rs1057519942
NM_006767.4(LZTR1):c.955del (p.Gln319fs) rs1386054181
NM_012082.4(ZFPM2):c.1168A>C (p.Lys390Gln) rs536096943
NM_012082.4(ZFPM2):c.130G>A (p.Glu44Lys) rs569356297
NM_012082.4(ZFPM2):c.1396_1399dup (p.Tyr467fs) rs1814012663
NM_012082.4(ZFPM2):c.2164G>C (p.Ala722Pro)
NM_012082.4(ZFPM2):c.2527A>G (p.Thr843Ala) rs121908604
NM_012082.4(ZFPM2):c.3335G>A (p.Ser1112Asn) rs763181942
NM_012082.4(ZFPM2):c.349C>T (p.Arg117Ter)
NM_012082.4(ZFPM2):c.757_761dup (p.Cys255fs) rs1813907455
NM_033419.5(PGAP3):c.851A>G (p.His284Arg) rs776720232
NM_133433.4(NIPBL):c.1811_1812del (p.Lys603_Ser604insTer) rs1057518944
NM_207361.5(FREM2):c.[4031G>A];[4558C>T]
NM_207361.6(FREM2):c.4994C>T (p.Ser1665Phe) rs1555261576
NM_207361.6(FREM2):c.5940_5942del (p.Leu1981del) rs775394591

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