ClinVar Miner

List of variants in gene TFAP2B reported as uncertain significance for arterial duct anomaly

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
Download table as spreadsheet
HGVS dbSNP
NM_003221.3(TFAP2B):c.-106A>T rs749242065
NM_003221.3(TFAP2B):c.-83G>A rs886061563
NM_003221.4(TFAP2B):c.*1199A>G rs886061578
NM_003221.4(TFAP2B):c.*1223A>G rs886061579
NM_003221.4(TFAP2B):c.*135_*136del rs140657288
NM_003221.4(TFAP2B):c.*136T>G rs2982621
NM_003221.4(TFAP2B):c.*1427del rs886061580
NM_003221.4(TFAP2B):c.*1644del rs886061581
NM_003221.4(TFAP2B):c.*1742T>C rs886061582
NM_003221.4(TFAP2B):c.*1765T>C rs886061583
NM_003221.4(TFAP2B):c.*2003A>G rs886061585
NM_003221.4(TFAP2B):c.*2200C>T rs886061586
NM_003221.4(TFAP2B):c.*2218T>A rs545250166
NM_003221.4(TFAP2B):c.*2497C>G rs886061587
NM_003221.4(TFAP2B):c.*2778T>C rs886061588
NM_003221.4(TFAP2B):c.*3078C>G rs886061589
NM_003221.4(TFAP2B):c.*3096A>G rs886061590
NM_003221.4(TFAP2B):c.*369C>T rs886061571
NM_003221.4(TFAP2B):c.*3725C>A rs770622965
NM_003221.4(TFAP2B):c.*3955G>C rs12374644
NM_003221.4(TFAP2B):c.*3995T>C rs201889632
NM_003221.4(TFAP2B):c.*4165G>T rs534021085
NM_003221.4(TFAP2B):c.*477C>T rs762515397
NM_003221.4(TFAP2B):c.*60T>A rs886061569
NM_003221.4(TFAP2B):c.*910_*911del rs35732696
NM_003221.4(TFAP2B):c.*910_*911insC rs1554165384
NM_003221.4(TFAP2B):c.*911_*915del rs770818655
NM_003221.4(TFAP2B):c.*911del rs35732696
NM_003221.4(TFAP2B):c.*912_*913CA[5] rs35649205
NM_003221.4(TFAP2B):c.*912_*913CA[6] rs35649205
NM_003221.4(TFAP2B):c.*912_*913CA[8] rs35649205
NM_003221.4(TFAP2B):c.*912_*916del rs886061577
NM_003221.4(TFAP2B):c.1235C>G (p.Ala412Gly) rs886061566
NM_003221.4(TFAP2B):c.1267G>C (p.Glu423Gln) rs886061567
NM_003221.4(TFAP2B):c.360T>C (p.Ser120=) rs886061564
NM_003221.4(TFAP2B):c.406G>C (p.Asp136His) rs139904414
NM_003221.4(TFAP2B):c.48T>G (p.Leu16=) rs371608614
NM_003221.4(TFAP2B):c.522C>G (p.Pro174=) rs886061565
NM_003221.4(TFAP2B):c.540+7ACAA[7] rs368226832

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.