List of variants in gene ALG13 reported as benign by Ambry 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001099922.3(ALG13):c.1435+5A>T	rs5985638	0.26139
NM_001099922.3(ALG13):c.1293A>G (p.Pro431=)	rs7063657	0.10892
NM_001099922.3(ALG13):c.1266T>C (p.Gly422=)	rs5985637	0.01375
NM_001099922.3(ALG13):c.183C>T (p.Tyr61=)	rs146925326	0.00950
NM_001099922.3(ALG13):c.1152G>A (p.Ala384=)	rs145353928	0.00643
NM_001099922.3(ALG13):c.3039A>G (p.Val1013=)	rs183032531	0.00394
NM_001099922.3(ALG13):c.2672C>T (p.Ser891Phe)	rs200066623	0.00390
NM_001099922.3(ALG13):c.2248-4A>G	rs370438099	0.00325
NM_001099922.3(ALG13):c.2617G>C (p.Ala873Pro)	rs142841538	0.00166
NM_001099922.3(ALG13):c.3414A>C (p.Ter1138Tyr)	rs201820102	0.00089
NM_001099922.3(ALG13):c.3093A>G (p.Gln1031=)	rs372260338	0.00065
NM_001099922.3(ALG13):c.108A>G (p.Arg36=)	rs769838471	0.00005
NM_001099922.3(ALG13):c.1641A>G (p.Gln547=)	rs768589790	0.00001
NM_001099922.3(ALG13):c.2754ACC[16] (p.Pro945dup)	rs750710267
NM_001099922.3(ALG13):c.2797CCT[12] (p.Pro945del)	rs56717389

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