List of variants in gene ALPL reported by Institute of Human Genetics, University of Wuerzburg

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.-176C>T	rs990367929	0.00007
NM_000478.6(ALPL):c.283G>A (p.Val95Met)	rs139811782	0.00002
NM_000478.6(ALPL):c.1078G>A (p.Gly360Arg)	rs749989499	0.00001
NM_000478.6(ALPL):c.1403C>T (p.Ala468Val)	rs766656419	0.00001
NM_000478.6(ALPL):c.1454C>T (p.Ala485Val)	rs886044912	0.00001
NM_000478.6(ALPL):c.1462G>A (p.Ala488Thr)	rs1570310172	0.00001
NM_000478.6(ALPL):c.530C>T (p.Ala177Val)	rs1114167438	0.00001
NM_000478.6(ALPL):c.*7A>G	rs753716865
NM_000478.6(ALPL):c.1114_1115del (p.Leu372fs)	rs1553414600
NM_000478.6(ALPL):c.1207A>T (p.Ser403Cys)	rs1216428237
NM_000478.6(ALPL):c.1309+13G>A	rs1397669293
NM_000478.6(ALPL):c.1451T>G (p.Met484Arg)	rs1558558939
NM_000478.6(ALPL):c.1558_1559del (p.Leu520fs)	rs1553415164
NM_000478.6(ALPL):c.472+5G>C	rs1558549099
NM_000478.6(ALPL):c.793-10T>C	rs1114167436
NM_000478.6(ALPL):c.876_882delinsT (p.Gly293_Asp294del)	rs1553414078

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