ClinVar Miner

List of variants in gene GATA4 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP gnomAD frequency
NM_001308093.3(GATA4):c.1224A>C (p.Pro408=) rs7830178 0.00435
NM_001308093.3(GATA4):c.825C>T (p.Cys275=) rs55980825 0.00275
NM_001308093.3(GATA4):c.462C>T (p.Phe154=) rs56348550 0.00232
NM_001308093.3(GATA4):c.1140C>T (p.Ser380=) rs34393445 0.00161
NM_001308093.3(GATA4):c.735C>T (p.Tyr245=) rs146696080 0.00148
NM_001308093.3(GATA4):c.1040C>T (p.Ala347Val) rs115372595 0.00144
NM_001308093.3(GATA4):c.888C>T (p.Cys296=) rs143109496 0.00083
NM_001308093.3(GATA4):c.348C>T (p.Ser116=) rs772532276 0.00044
NM_001308093.3(GATA4):c.918C>T (p.Pro306=) rs147050993 0.00044
NM_001308093.3(GATA4):c.531C>A (p.Ala177=) rs573733348 0.00034
NM_001308093.3(GATA4):c.1001-4C>G rs199915980 0.00024
NM_001308093.3(GATA4):c.72C>G (p.Gly24=) rs746574040 0.00022
NM_001308093.3(GATA4):c.726C>T (p.Cys242=) rs1062215 0.00021
NM_001308093.3(GATA4):c.585G>C (p.Arg195=) rs1040398846 0.00019
NM_001308093.3(GATA4):c.630C>T (p.Asp210=) rs192122549 0.00019
NM_001308093.3(GATA4):c.1029C>T (p.Pro343=) rs368098911 0.00015
NM_001308093.3(GATA4):c.90G>A (p.Ala30=) rs768982638 0.00014
NM_001308093.3(GATA4):c.1125C>T (p.Tyr375=) rs56330552 0.00013
NM_001308093.3(GATA4):c.246C>A (p.Thr82=) rs1037655842 0.00011
NM_001308093.3(GATA4):c.1152G>A (p.Thr384=) rs147958528 0.00010
NM_001308093.3(GATA4):c.15G>A (p.Leu5=) rs55635838 0.00010
NM_001308093.3(GATA4):c.1167G>A (p.Ala389=) rs55968178 0.00009
NM_001308093.3(GATA4):c.13T>C (p.Leu5=) rs55670878 0.00007
NM_001308093.3(GATA4):c.127C>A (p.Arg43=) rs387906770 0.00006
NM_001308093.3(GATA4):c.330C>T (p.Phe110=) rs779273192 0.00006
NM_001308093.3(GATA4):c.609C>T (p.Pro203=) rs1210009123 0.00006
NM_001308093.3(GATA4):c.1236G>A (p.Ala412=) rs771755685 0.00004
NM_001308093.3(GATA4):c.1311C>T (p.His437=) rs779684582 0.00004
NM_001308093.3(GATA4):c.747C>T (p.Asn249=) rs140212153 0.00004
NM_001308093.3(GATA4):c.789C>T (p.Ser263=) rs777744927 0.00004
NM_001308093.3(GATA4):c.1206G>A (p.Ser402=) rs141909277 0.00003
NM_001308093.3(GATA4):c.762G>A (p.Pro254=) rs143454176 0.00003
NM_001308093.3(GATA4):c.804G>A (p.Val268=) rs774926374 0.00003
NM_001308093.3(GATA4):c.195C>T (p.Gly65=) rs752600136 0.00002
NM_001308093.3(GATA4):c.909C>T (p.His303=) rs201516339 0.00002
NM_001308093.3(GATA4):c.1008A>G (p.Ser336=) rs752425131 0.00001
NM_001308093.3(GATA4):c.1077C>T (p.Ser359=) rs375407669 0.00001
NM_001308093.3(GATA4):c.1200C>A (p.Val400=) rs778818575 0.00001
NM_001308093.3(GATA4):c.159C>T (p.Tyr53=) rs1258554563 0.00001
NM_001308093.3(GATA4):c.234G>A (p.Ala78=) rs756850527 0.00001
NM_001308093.3(GATA4):c.645C>T (p.Gly215=) rs1411266373 0.00001
NM_001308093.3(GATA4):c.768C>A (p.Ile256=) rs760250504 0.00001
NM_001308093.3(GATA4):c.855C>T (p.Arg285=) rs758475308 0.00001
NM_001308093.3(GATA4):c.1017G>A (p.Glu339=)
NM_001308093.3(GATA4):c.1056C>T (p.Ser352=)
NM_001308093.3(GATA4):c.105G>T (p.Ser35=)
NM_001308093.3(GATA4):c.1089T>A (p.Arg363=) rs143385784
NM_001308093.3(GATA4):c.1089T>C (p.Arg363=) rs143385784
NM_001308093.3(GATA4):c.1101G>C (p.Thr367=) rs771381966
NM_001308093.3(GATA4):c.1128G>A (p.Gly376=) rs781488882
NM_001308093.3(GATA4):c.1188C>T (p.Ser396=)
NM_001308093.3(GATA4):c.1191C>T (p.Ile397=)
NM_001308093.3(GATA4):c.1210C>T (p.Leu404=)
NM_001308093.3(GATA4):c.1218C>T (p.Leu406=)
NM_001308093.3(GATA4):c.1254T>C (p.Ser418=) rs1060503828
NM_001308093.3(GATA4):c.1290C>T (p.Ser430=)
NM_001308093.3(GATA4):c.1328C>G (p.Ala443Gly) rs146017816
NM_001308093.3(GATA4):c.150C>A (p.Gly50=)
NM_001308093.3(GATA4):c.177G>A (p.Ala59=)
NM_001308093.3(GATA4):c.189C>T (p.Ser63=)
NM_001308093.3(GATA4):c.240C>A (p.Pro80=)
NM_001308093.3(GATA4):c.24C>A (p.Ala8=)
NM_001308093.3(GATA4):c.309G>T (p.Pro103=)
NM_001308093.3(GATA4):c.318G>A (p.Pro106=)
NM_001308093.3(GATA4):c.333G>A (p.Pro111=) rs1331416104
NM_001308093.3(GATA4):c.366C>A (p.Ala122=)
NM_001308093.3(GATA4):c.369T>C (p.Ala123=)
NM_001308093.3(GATA4):c.378C>A (p.Ala126=)
NM_001308093.3(GATA4):c.379C>A (p.Arg127=)
NM_001308093.3(GATA4):c.420T>G (p.Gly140=) rs886038808
NM_001308093.3(GATA4):c.423G>A (p.Ala141=) rs1404734578
NM_001308093.3(GATA4):c.432G>A (p.Ala144=)
NM_001308093.3(GATA4):c.444G>A (p.Gln148=) rs1352635163
NM_001308093.3(GATA4):c.489G>C (p.Pro163=)
NM_001308093.3(GATA4):c.492T>C (p.Ala164=)
NM_001308093.3(GATA4):c.513G>A (p.Ala171=)
NM_001308093.3(GATA4):c.51C>T (p.Ala17=)
NM_001308093.3(GATA4):c.525A>G (p.Ala175=)
NM_001308093.3(GATA4):c.543C>A (p.Ala181=) rs544097659
NM_001308093.3(GATA4):c.543C>G (p.Ala181=) rs544097659
NM_001308093.3(GATA4):c.543C>T (p.Ala181=) rs544097659
NM_001308093.3(GATA4):c.561G>A (p.Pro187=)
NM_001308093.3(GATA4):c.567G>A (p.Leu189=) rs1554488672
NM_001308093.3(GATA4):c.597C>G (p.Ala199=)
NM_001308093.3(GATA4):c.603A>C (p.Arg201=)
NM_001308093.3(GATA4):c.807C>G (p.Gly269=)
NM_001308093.3(GATA4):c.840C>A (p.Thr280=)
NM_001308093.3(GATA4):c.85G>A (p.Gly29Ser)
NM_001308093.3(GATA4):c.903G>A (p.Lys301=) rs1585687961
NM_001308093.3(GATA4):c.934C>A (p.Arg312=) rs138404762
NM_001308093.3(GATA4):c.966G>A (p.Lys322=) rs995668697

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