ClinVar Miner

List of variants in gene TGFBR2 reported as uncertain significance by Invitae

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Total variants: 69
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HGVS dbSNP
NM_003242.6(TGFBR2):c.1006T>G (p.Tyr336Asp) rs104893812
NM_003242.6(TGFBR2):c.1015C>T (p.Arg339Trp) rs761991787
NM_003242.6(TGFBR2):c.1016G>C (p.Arg339Pro) rs727503473
NM_003242.6(TGFBR2):c.1043G>A (p.Arg348His) rs369450067
NM_003242.6(TGFBR2):c.1058C>T (p.Ser353Phe) rs1553630235
NM_003242.6(TGFBR2):c.1126G>A (p.Val376Met) rs755967723
NM_003242.6(TGFBR2):c.1130A>G (p.His377Arg) rs1553630274
NM_003242.6(TGFBR2):c.1135_1140del (p.Asp379_Leu380del) rs1553630282
NM_003242.6(TGFBR2):c.1151A>G (p.Asn384Ser) rs193922660
NM_003242.6(TGFBR2):c.1152T>A (p.Asn384Lys) rs193922661
NM_003242.6(TGFBR2):c.1153A>G (p.Ile385Val) rs137908708
NM_003242.6(TGFBR2):c.1159G>T (p.Val387Leu) rs35766612
NM_003242.6(TGFBR2):c.1163A>G (p.Lys388Arg) rs193922662
NM_003242.6(TGFBR2):c.116C>A (p.Thr39Asn) rs146277116
NM_003242.6(TGFBR2):c.1181G>A (p.Cys394Tyr) rs1553630289
NM_003242.6(TGFBR2):c.1189G>T (p.Asp397Tyr)
NM_003242.6(TGFBR2):c.1202C>T (p.Ser401Phe)
NM_003242.6(TGFBR2):c.1219A>G (p.Thr407Ala) rs1559467311
NM_003242.6(TGFBR2):c.1246A>G (p.Ser416Gly) rs1060501983
NM_003242.6(TGFBR2):c.1254+6T>A rs1026852885
NM_003242.6(TGFBR2):c.1273A>C (p.Met425Leu)
NM_003242.6(TGFBR2):c.1274T>C (p.Met425Thr) rs1553630438
NM_003242.6(TGFBR2):c.1301T>C (p.Met434Thr)
NM_003242.6(TGFBR2):c.1334C>A (p.Thr445Asn) rs886038936
NM_003242.6(TGFBR2):c.1340T>A (p.Val447Asp)
NM_003242.6(TGFBR2):c.1408T>A (p.Tyr470Asn)
NM_003242.6(TGFBR2):c.1436G>A (p.Arg479Gln) rs1553631704
NM_003242.6(TGFBR2):c.1459A>C (p.Met487Leu)
NM_003242.6(TGFBR2):c.1492C>G (p.Pro498Ala) rs1553631720
NM_003242.6(TGFBR2):c.1510T>C (p.Trp504Arg)
NM_003242.6(TGFBR2):c.151T>C (p.Cys51Arg) rs1559456531
NM_003242.6(TGFBR2):c.1524+7A>G rs1553631728
NM_003242.6(TGFBR2):c.1525-6C>G rs748388518
NM_003242.6(TGFBR2):c.1525G>A (p.Gly509Ser)
NM_003242.6(TGFBR2):c.1526G>T (p.Gly509Val) rs863223853
NM_003242.6(TGFBR2):c.1537del (p.Val513fs)
NM_003242.6(TGFBR2):c.1547C>T (p.Thr516Met) rs149847376
NM_003242.6(TGFBR2):c.1563G>A (p.Trp521Ter) rs1553631968
NM_003242.6(TGFBR2):c.1564G>A (p.Asp522Asn) rs863223854
NM_003242.6(TGFBR2):c.1565A>C (p.Asp522Ala) rs886038768
NM_003242.6(TGFBR2):c.1576G>C (p.Glu526Gln) rs121918714
NM_003242.6(TGFBR2):c.15_25dup (p.Leu9fs) rs1559443652
NM_003242.6(TGFBR2):c.1643C>T (p.Ser548Leu) rs755070814
NM_003242.6(TGFBR2):c.1697C>G (p.Thr566Ser)
NM_003242.6(TGFBR2):c.1701A>G (p.Lys567=) rs763371077
NM_003242.6(TGFBR2):c.175T>C (p.Ser59Pro) rs1559456557
NM_003242.6(TGFBR2):c.202A>C (p.Met68Leu) rs1060501985
NM_003242.6(TGFBR2):c.215G>A (p.Ser72Asn) rs764941621
NM_003242.6(TGFBR2):c.264-5T>G rs1315800025
NM_003242.6(TGFBR2):c.367A>T (p.Met123Leu) rs768385200
NM_003242.6(TGFBR2):c.383dup (p.Pro129fs)
NM_003242.6(TGFBR2):c.394A>G (p.Thr132Ala) rs146497045
NM_003242.6(TGFBR2):c.412T>G (p.Cys138Gly) rs863223838
NM_003242.6(TGFBR2):c.448T>C (p.Ser150Pro) rs1346274891
NM_003242.6(TGFBR2):c.4G>T (p.Gly2Cys) rs565502802
NM_003242.6(TGFBR2):c.500T>C (p.Val167Ala) rs779052721
NM_003242.6(TGFBR2):c.511A>G (p.Ser171Gly) rs767581059
NM_003242.6(TGFBR2):c.556T>A (p.Phe186Ile) rs368346624
NM_003242.6(TGFBR2):c.617C>T (p.Thr206Met) rs150022335
NM_003242.6(TGFBR2):c.645C>G (p.His215Gln) rs758827786
NM_003242.6(TGFBR2):c.659T>C (p.Leu220Pro) rs1553630112
NM_003242.6(TGFBR2):c.673T>C (p.Ser225Pro)
NM_003242.6(TGFBR2):c.760C>T (p.Arg254Cys) rs863223856
NM_003242.6(TGFBR2):c.832A>T (p.Ile278Phe) rs1559466871
NM_003242.6(TGFBR2):c.869A>G (p.Glu290Gly)
NM_003242.6(TGFBR2):c.907A>C (p.Asn303His)
NM_003242.6(TGFBR2):c.914T>G (p.Leu305Arg) rs1553630174
NM_003242.6(TGFBR2):c.938G>A (p.Arg313Gln)
NM_003242.6(TGFBR2):c.95-3C>A rs375330013

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