ClinVar Miner

List of variants in gene FGD4 studied for not provided

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Total variants: 73
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HGVS dbSNP
GRCh37/hg19 12p11.21(chr12:32608165-32825558)x1
GRCh37/hg19 12p11.21(chr12:32616797-32713135)x1
NM_001304481.1(FGD4):c.220C>A (p.Pro74Thr) rs199744649
NM_001304481.1(FGD4):c.222C>A (p.Pro74=) rs1465471003
NM_001370298.3(FGD4):c.1769A>C (p.Tyr590Ser)
NM_001370298.3(FGD4):c.1808_1809del (p.Thr603fs) rs886039361
NM_001370298.3(FGD4):c.1961A>G (p.Gln654Arg)
NM_001370298.3(FGD4):c.2173-322del rs150852537
NM_001370298.3(FGD4):c.2298_2302del (p.Lys767fs) rs751035912
NM_001370298.3(FGD4):c.2298_2302dup (p.Gly768fs) rs751035912
NM_001370298.3(FGD4):c.2509C>A (p.Pro837Thr)
NM_001370298.3(FGD4):c.2602T>C (p.Trp868Arg)
NM_001370298.3(FGD4):c.658C>T (p.Gln220Ter)
NM_139241.3(FGD4):c.-245-29728T>C rs561223009
NM_139241.3(FGD4):c.-92-339A>G rs73305550
NM_139241.3(FGD4):c.1097T>C (p.Leu366Ser) rs555510533
NM_139241.3(FGD4):c.1132+8_1132+9insG rs1555216986
NM_139241.3(FGD4):c.1133-135G>A rs10844252
NM_139241.3(FGD4):c.1133-236T>G rs1004968
NM_139241.3(FGD4):c.1203G>C (p.Lys401Asn) rs1131691394
NM_139241.3(FGD4):c.1278A>C (p.Glu426Asp) rs879254000
NM_139241.3(FGD4):c.1329C>A (p.Tyr443Ter) rs886041200
NM_139241.3(FGD4):c.1338+200A>C rs10844254
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1398A>T (p.Thr466=) rs1220106574
NM_139241.3(FGD4):c.1431A>G (p.Lys477=) rs1023207495
NM_139241.3(FGD4):c.1494A>G (p.Thr498=) rs572887361
NM_139241.3(FGD4):c.1515T>C (p.Ser505=) rs60803891
NM_139241.3(FGD4):c.1560C>T (p.Ile520=) rs61748364
NM_139241.3(FGD4):c.1562A>G (p.Asp521Gly) rs141237776
NM_139241.3(FGD4):c.1635+221T>A rs12303795
NM_139241.3(FGD4):c.1636-292C>T rs11052111
NM_139241.3(FGD4):c.1711C>A (p.Pro571Thr) rs144693221
NM_139241.3(FGD4):c.1711C>G (p.Pro571Ala) rs144693221
NM_139241.3(FGD4):c.1712C>A (p.Pro571His) rs145071617
NM_139241.3(FGD4):c.1721C>T (p.Ala574Val) rs1341534652
NM_139241.3(FGD4):c.1722A>G (p.Ala574=) rs771910342
NM_139241.3(FGD4):c.1730G>A (p.Arg577Gln)
NM_139241.3(FGD4):c.1758A>C (p.Gly586=) rs200761894
NM_139241.3(FGD4):c.1761+200G>A rs1909510
NM_139241.3(FGD4):c.1761+8A>T rs761674021
NM_139241.3(FGD4):c.1762-23T>G rs76834265
NM_139241.3(FGD4):c.1762-257C>T rs11831099
NM_139241.3(FGD4):c.1878A>C (p.Glu626Asp)
NM_139241.3(FGD4):c.2005dup (p.Gln669fs) rs1555224772
NM_139241.3(FGD4):c.2044-10T>C rs1592514932
NM_139241.3(FGD4):c.2044-236G>A rs10771973
NM_139241.3(FGD4):c.2044-46A>G rs74073032
NM_139241.3(FGD4):c.2149G>A (p.Val717Met) rs61753359
NM_139241.3(FGD4):c.2176G>T (p.Glu726Ter) rs771529170
NM_139241.3(FGD4):c.2214T>C (p.Ala738=) rs200144770
NM_139241.3(FGD4):c.236C>T (p.Thr79Ile) rs145115430
NM_139241.3(FGD4):c.255A>T (p.Ala85=) rs139357821
NM_139241.3(FGD4):c.329T>C (p.Leu110Pro) rs142609007
NM_139241.3(FGD4):c.381A>G (p.Ile127Met) rs774466701
NM_139241.3(FGD4):c.479G>A (p.Gly160Asp) rs201826412
NM_139241.3(FGD4):c.484G>C (p.Gly162Arg) rs774679169
NM_139241.3(FGD4):c.50C>G (p.Pro17Arg) rs371407163
NM_139241.3(FGD4):c.569T>A (p.Leu190Gln) rs144980336
NM_139241.3(FGD4):c.57G>A (p.Lys19=) rs1427707678
NM_139241.3(FGD4):c.597G>C (p.Met199Ile) rs1592295526
NM_139241.3(FGD4):c.601-154T>G rs12299653
NM_139241.3(FGD4):c.670C>T (p.Arg224Ter) rs118203972
NM_139241.3(FGD4):c.759C>A (p.Ile253=) rs1592364946
NM_139241.3(FGD4):c.836+10G>T rs41276676
NM_139241.3(FGD4):c.837-149T>G rs4931640
NM_139241.3(FGD4):c.837-37T>A rs4931641
NM_139241.3(FGD4):c.873A>G (p.Lys291=) rs1224103433
NM_139241.3(FGD4):c.952_953del (p.Glu318fs) rs771606350
NM_139241.3(FGD4):c.955C>T (p.Arg319Cys) rs1131691854
NM_139241.3(FGD4):c.991del (p.Gln331fs) rs1393673267
NM_139241.3(FGD4):c.993+149T>C rs7964734
NM_139241.3(FGD4):c.994-7A>G

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