Variants in gene ALPL with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.330= (p.Ser110=)	rs1780316	0.07689
NM_000478.6(ALPL):c.1189+19G>T	rs61778393	0.02227
NM_000478.6(ALPL):c.1542G>T (p.Ala514=)	rs3200256	0.01113
NM_000478.6(ALPL):c.1381G>A (p.Val461Ile)	rs34810399	0.00860
NM_000478.6(ALPL):c.1119C>T (p.Thr373=)	rs112335417	0.00852
NM_000478.6(ALPL):c.455G>A (p.Arg152His)	rs149344982	0.00814
NM_000478.6(ALPL):c.859T>C (p.Leu287=)	rs141742288	0.00141
NM_000478.6(ALPL):c.473-12C>T	rs147181132	0.00137
NM_000478.6(ALPL):c.182-15C>G	rs201873253	0.00109
NM_000478.6(ALPL):c.818C>T (p.Thr273Met)	rs148405563	0.00106
NM_000478.6(ALPL):c.997+11C>T	rs187255765	0.00105
NM_000478.6(ALPL):c.1482C>T (p.Leu494=)	rs142545037	0.00102
NM_000478.6(ALPL):c.744C>T (p.Asp248=)	rs188689330	0.00047
NM_000478.6(ALPL):c.858A>G (p.Leu286=)	rs375027534	0.00006
NM_000478.6(ALPL):c.472+12del	rs35423948
NM_000478.6(ALPL):c.534C>T (p.Tyr178=)	rs201250289

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.