ClinVar Miner

List of variants in gene TCF4 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.145+123C>T rs599550 0.90304
NM_001083962.2(TCF4):c.789+23C>T rs1788027 0.53241
NM_001083962.2(TCF4):c.1941A>G (p.Ser647=) rs8766 0.37317
NM_001083962.2(TCF4):c.1147-69A>G rs62092442 0.35321
NM_001083962.2(TCF4):c.1146+229G>C rs11662842 0.34432
NM_001083962.2(TCF4):c.146-46302A>G rs9957668 0.33791
NM_001083962.2(TCF4):c.146-46406C>G rs9964328 0.33296
NM_001083962.2(TCF4):c.1350+122G>A rs1539950 0.25109
NM_001083962.2(TCF4):c.1350+55A>G rs1539951 0.25072
NM_001083962.2(TCF4):c.1880-65G>A rs10221362 0.23932
NM_001083962.2(TCF4):c.1146+198A>G rs11664992 0.23539
NM_001083962.2(TCF4):c.305-165C>T rs17522826 0.15868
NM_001083962.2(TCF4):c.145+226C>T rs12455881 0.13747
NM_001083962.2(TCF4):c.73-306G>A rs34603418 0.13399
NM_001083962.2(TCF4):c.1486+172T>C rs41483647 0.10978
NM_001083962.2(TCF4):c.1879+75T>C rs8087570 0.10953
NM_001083962.2(TCF4):c.1879+78T>C rs8087569 0.10952
NM_001083962.2(TCF4):c.1650-323C>A rs41339445 0.10925
NM_001083962.2(TCF4):c.991-142A>G rs35969244 0.10330
NM_001083962.2(TCF4):c.990+179_990+182dup rs149477248 0.08588
NM_001083962.2(TCF4):c.*4+34C>T rs6567210 0.08009
NM_001083962.2(TCF4):c.208-122C>A rs73479266 0.06459
NM_001083962.2(TCF4):c.990+192C>T rs3817527 0.04802
NM_001083962.2(TCF4):c.1879+216G>A rs11152294 0.04445
NM_001083962.2(TCF4):c.550-190C>T rs1787791 0.04038
NM_001083962.2(TCF4):c.72+248C>T rs75754713 0.03951
NM_001083962.2(TCF4):c.656-116C>G rs1787793 0.03771
NM_001083962.2(TCF4):c.1147-76G>A rs62092443 0.03622
NM_001083962.2(TCF4):c.1350+281C>A rs62092441 0.03579
NM_001083962.2(TCF4):c.923-224C>T rs73957090 0.03481
NM_001083962.2(TCF4):c.550-101G>A rs57421596 0.02755
NM_001083962.2(TCF4):c.*4088T>C rs182171482 0.00632
NM_001083962.2(TCF4):c.1905G>A (p.Ala635=) rs151150677 0.00274
NM_001083962.2(TCF4):c.*549G>A rs148367822 0.00265
NM_001083962.2(TCF4):c.*1763C>A rs556687934 0.00103
NM_001083962.2(TCF4):c.1923G>A (p.Glu641=) rs76956936 0.00067
NM_001083962.2(TCF4):c.341G>A (p.Arg114Lys) rs139876825 0.00043
NM_001083962.2(TCF4):c.330A>C (p.Ser110=) rs780528611 0.00016
NM_001083962.2(TCF4):c.990+12T>C rs144346949 0.00016
NM_001083962.2(TCF4):c.1650-14C>T rs569480730 0.00002
NM_001083962.2(TCF4):c.1486+6T>C rs547850991 0.00001
NM_001083962.2(TCF4):c.639C>T (p.Ser213=) rs771829952 0.00001
GRCh37/hg19 18q21.2(chr18:53234540-53237513)x3
NM_001083962.2(TCF4):c.*4214GTTTTT[3] rs571078805
NM_001083962.2(TCF4):c.-160CGG[8] rs886053961
NM_001083962.2(TCF4):c.1069+30A>G rs143555588
NM_001083962.2(TCF4):c.1419G>T (p.Pro473=) rs143944746
NM_001083962.2(TCF4):c.146-120G>T rs3760600
NM_001083962.2(TCF4):c.146-46372T>A rs9954890
NM_001083962.2(TCF4):c.146-46693C>T rs67387556
NM_001083962.2(TCF4):c.1650-202C>T rs2276195
NM_001083962.2(TCF4):c.207+73TC[14] rs1555671780
NM_001083962.2(TCF4):c.207+97_207+104del rs143184224
NM_001083962.2(TCF4):c.207+98CA[14] rs151196106
NM_001083962.2(TCF4):c.207+98CA[17] rs151196106
NM_001083962.2(TCF4):c.207+98CA[18] rs151196106
NM_001083962.2(TCF4):c.207+98_207+99insCTCA rs867214369
NM_001083962.2(TCF4):c.369+1365del
NM_001083962.2(TCF4):c.549+28099AG[2] rs142035505
NM_001083962.2(TCF4):c.72+204del rs34071688
NM_003199.2(TCF4):c.-312dup

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