List of variants in gene ALPL reported as likely benign by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
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.-104-5T>C	rs184586988	0.00097
NM_000478.6(ALPL):c.468C>T (p.Asp156=)	rs143621566	0.00052
NM_000478.6(ALPL):c.1455G>A (p.Ala485=)	rs188443578	0.00009
NM_000478.6(ALPL):c.1056G>A (p.Ala352=)	rs774824768	0.00006
NM_000478.6(ALPL):c.1446C>T (p.His482=)	rs747980975	0.00006
NM_000478.6(ALPL):c.918C>T (p.Asp306=)	rs373257447	0.00005
NM_000478.6(ALPL):c.339C>T (p.Thr113=)	rs377453516	0.00003
NM_000478.6(ALPL):c.528C>T (p.Ala176=)	rs758330265	0.00003
NM_000478.6(ALPL):c.863-15T>C	rs373980626	0.00003
NM_000478.6(ALPL):c.1437C>T (p.Tyr479=)	rs527657489	0.00002
NM_000478.6(ALPL):c.863-8C>T	rs775518662	0.00002
NM_000478.6(ALPL):c.1047G>T (p.Leu349=)	rs771632536	0.00001
NM_000478.6(ALPL):c.1143C>T (p.His381=)	rs749419329	0.00001
NM_000478.6(ALPL):c.282C>T (p.Phe94=)	rs746608270	0.00001
NM_000478.6(ALPL):c.297+9C>A	rs773328385	0.00001
NM_000478.6(ALPL):c.582T>C (p.Pro194=)	rs112063292	0.00001
NM_000478.6(ALPL):c.660G>T (p.Gly220=)	rs1558552231	0.00001
NM_000478.6(ALPL):c.1189+11C>T	rs201272867
NM_000478.6(ALPL):c.1310-5C>T	rs755472353
NM_000478.6(ALPL):c.1419C>T (p.Gly473=)	rs373417343
NM_000478.6(ALPL):c.393C>T (p.Ser131=)	rs2148158625

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